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Choanal atresia Radiology

Choanal atresia may be unilateral or bilateral. In this case, there is bony narrowing with mucosal obstruction of the choana bilaterally causing respiratory distress and requiring intubation and ventilation. The patient proceeded to surgery and made an uncomplicated recovery. 1 article features images from this cas Computed tomography facilitates the diagnosis of children with choanal atresia. This modality defines the full anatomic abnormality of bony choanal atresia: medial bowing and thickening of the lateral wall of the nasal cavity, enlargement of the vomer, and fusion of these elements

Choanal atresia is a congenital obstruction of the posterior nasal apertures. It is a very rare condition usually associated with syndromes and diagnosed postnatally. Prenatal diagnosis is very difficult, but choanal atresia can be suspected in the presence of nasal septal deviation or single nostril Choanal atresia refers to a lack of formation of the choanal openings. Bilateral typically present soon after birth with neonatal respiratory distress. Unilateral choanal atresias present later and can be relatively asymptomatic or present with rhinorrhea and represent 2/3 of cases Cases of Choanal Atresia AP + lateral radiographs of the airway after the injection of contrast into the nares bilaterally shows no passage of contrast into the oropharynx with the obstruction at the level of the vomer The evaluation of choanal atresia by computed tomography International Journal of Pediatric Otorhinolaryngology, Vol. 12, No. 1 Computed tomography of choanal atresia: special considerations of the unilateral typ

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Choanal atresia: precise CT evaluation

  1. Choanal atresia is the commonest congenital abnormality of the nose. It can be unilateral or bilateral, with either a bony (85%) or membranous (15%) obstruction at the posterior limit of the nasal septum. It occurs in 1:7000 births, and there is a family tendency
  2. CT scanning is the radiographic procedure of choice in the evaluation of choanal atresia. For good results, careful suctioning is performed to clear excess mucus, and a topical decongestant is..
  3. Abstract Introduction: Choanal atresia (CA) is an infrequent congenital obliteration of the airway at the level of the posterior nasal aperture resulting in the absence of connection between the nasal cavity and the aerodigestive tract. We present our experience with an endoscopic technique for congenital CA without the use of intranasal stents
  4. Generally, choanal atresia may affect one or both Choanae, although most studies show that the unilateral form is more common than the bilateral one [2,3], and the incidence is higher in females than in males (2:1) [4,5].The unilateral form is frequently on the right side [2,5].Bilateral atresia is more commonly associated with syndromes such as CHARGE, Treacher-Collins, and Crouzon's.

Radiological studies have confirmed the clinical impression of bony atresia in all patients with unilateral posterior choanal atresia. All forms of radiological studies confirmed the clinical impression of mixed atresia in our patient (No.5) with bilateral choanal atresia Radiology. Starship Child Health Radiology Imaging Protocol. CT - Choanal Atresia. Date last published: 08 October 2020. CT - Choanal Atresia. This document is only valid for the day on which it is accessed. Please read our disclaimer. Radiology. Donate. Document Control; Indication Choanal atresia refers to the obstruction of one or both of these posterior choanae. This obstruction can be either bony or membranous. Because babies are obligate nose breathers, bilateral obstruction leads to severe respiratory distress. Unilateral choanal atresia, on the other hand, is ususally first diagnosed when the child is older In 1854, Emmert reported the first successful surgical procedure for congenital choanal atresia in a 7-year-old boy using a curved trocar transnasally.• Over the years, the necessity of serial dilatations to maintain patency of the choanae has been clearly recognized. 4 Choanal atresia is a blockage in the back of a baby's nose that makes it hard to breathe. It's often seen in newborns with other birth defects, such as Treacher Collins syndrome or CHARGE syndrome...

10. Williams HJ. Posterior choanal atresia. AJR 1971;112: 1-11 11. Fitz CR , Noyek AM. Contemporary radiology in congenital cra­ niofacial disorders. Otolaryngol Clin North Am 1981;14:65-81 12. Osborne AG, Mclff EB. Computed tomography of the nose. Head Neck Surg 1982;4: 182-199 13. Shirkhoda A, Biggers WP. Choanal atresia. Radiology 1982;142. Choanal atresia is a relatively rare congenital anomaly that occurs in 1 in 5,000 to 10,000 live births. The incidence in females is twice that of males. Approximately 50% of choanal atresia is bilateral, 29% of cases are purely bony, and 71% are mixed bony-membranous type Computed tomography (CT) scanning is the radiographic procedure of choice in the evaluation of choanal atresia. For good results, careful suctioning is performed to clear excess mucus, and a.. Bilateral choanal atresia in a 7-year-old boy: a case study. Ismail A(1), Abdulkadir AY. Author information: (1)Department of Radiology, Aminu Kano Teaching Hospital, Kano, Nigeria. ibnmalikana@yahoo.co.uk Choanal atresia is a developmental failure of the nasal cavity to communicate with nasopharynx Choanal atresia can be suspected prenatally in the presence of nose anomalies, mainly nasal septal deviation or the presence of a single nostril (Fig. 67.1). 3-6. Magnetic Resonance Imaging. Postnatal magnetic resonance imaging and computed tomography are the gold standard imaging techniques for diagnosis of choanal atresia

Choanal Atresia Radiology Ke

  1. Objective . To illustrate the role of multislice computed tomography and local contrast instillation in the diagnosis and characterization of choanal atresia. To review the common associated radiological findings. Methods . We analyzed 9 pediatric patients (5 males and 4 females) with suspected choanal atresia by multislice computed tomography
  2. This study was conducted by sophisticated head and neck radiology operating unit and pediatric department of a tertiary referral center. In the study, we included 19 patients with choanal atresia. The mean age of the children was 207 333 days; 14 were less than 1 year old and 5 between 1 and 3 years; 10 were females and 9 males; 5 were affected.
  3. Choanal atresia (CA) is a relatively uncommon but well-recognized condition characterized by the anatomical closure of the posterior choanae in the nasal cavity. Since the original description back in the early eighteenth century, there have been controversies regarding its exact pathogenesis, the optimal surgical approach, and the use of adjunct treatments such as post-surgical stenting and.
  4. Posterior choanal atresia is an uncommon condition, but it is not as rare as the scant radiologic literature would indicate. 2. The findings in 19 cases of unilateral and bilateral choanal atresia are presented, with the emphasis on symptoms, diagnosis, and treatment
  5. Developed by renowned radiologists in each specialty, STATdx provides comprehensive decision support you can rely on - Choanal Atresia. link. Bookmarks (0) Head and Neck. Diagnosis. Nose and Sinus. Congenital and Developmental Lesions. Choanal Atresia.
  6. Choanal atresia/stenosis is an important cause of airway obstruction. It can be unilateral or bilateral, boney or membranous. The etiology of choanal atresia/stenosis is not known. Medial bowing and thickening of the walls of the nasal cavity (perpendicular plate of palatine bone and the pterygoid process) or enlargement of the vomer leads to.

10.1055/b-0038-162805 8.18 Choanal Atresia Key Points Choanal atresia occurs in ~ 1 in 5,000 to 8,000 births. Bilateral atresia is more common and is associated with other anomalies (e.g., CHARGE association). Endoscopic techniques have greatly improved the safety of the transnasal approach. Choanal atresia is a congenital condition in which one or both of th Choanal Atresia. Choanal atresia is a congenital (present at birth) condition in which the back of the nasal passage (called the choana) is blocked, usually by abnormal bony or soft tissue that does not develop properly during fetal development. Normally the nasal passage forms in early development through a thick wall of soft tissue Congenital nasal pyriform aperture stenosis (CNPAS), first published in the radiology literature in 1988 and described clinically in 1989, 1 is one of the rare causes of neonatal airway obstruction, occurring at a frequency of one-fifth to one-third that of choanal atresia. 2 Congenital airway obstruction is a problem that affects up to 1 in 5000 infants. 1,3 A majority of these obstructions.

SUMMARY: Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth and/or development, Genital and/or urinary abnormalities, and Ear abnormalities and deafness (CHARGE) syndrome is a disorder with multiple congenital anomalies seen on imaging. A retrospective review of 10 patients with CHARGE syndrome who underwent MR imaging of the brain as part of a preoperative. Choanal atresia is a relatively rare congenital anomaly that occurs in 1 in 5,000 to 10,000 live births. The incidence in females is twice that of males. Approximately 50% of choanal atresia is bilateral, 29% of cases are purely bony, and 71% are mixed bony-membranous type. Choanal atresia is commonly associated with other congenital.

3. Pass a small red rubber feeding tube (catheter) along the ventral and common meatus of the nasopharynx (Video 34.2: Red rubber catheter test for choanal atresia). If the nasopharynx is open, the tube can be passed into the esophagus or trachea. If the nasopharynx is obstructed, the tube will stop, usually at the level of the eye Choanal atresia is a rare developmental condition that is defined as a narrowing or complete blockage of the nasal passages. Rapid surgical management is crucial in cases of bilateral choanal atresia since it may develop into a life-threatening emergency. We present the case of a full-term female newborn who developed mild respiratory distress soon after birth

International Journal of Pediatric Otorhinolaryngology, 11 (1986) 265-274 265 Elsevier POR 00377 Computed tomography in the evaluation of choanal atresia * Ralph F. Wetmore i and Soroosh Mahboubi 2 z Div&ion of Otolaryngology and Human Communication, and -' Department of Radiology, Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, Philadelphia PA (U.S.A. The Role of Computed Tomography in the Evaluation of Bilateral Choanal Atresia: Two Case Reports, Iran J Radiol. 2009 ; 6(4):e78858. ARTICLE INFORMATION Iranian Journal of Radiology: 6 (4) ; e7885 Congenital choanal atresia (CCA) is the developmental failure of the nasal cavity to communicate with the nasopharynx. The aim of this study was to investigate and analyse the CT findings in such cases. Seven patients with CCA were included in our study over a 3‐year period (2001-2004)

Congenital choanal atresia (CCA) is the developmental failure of the nasal cavity to communicate with the nasopharynx. The aim of this study was to investigate and analyse the CT findings in such cas.. Etiology and Pathophysiology. • Choanal atresia results from failure of the bucconasal membrane to separate from the primitive buccal or oral cavity from the nasal pits during embryologic development. • This membrane can be complete, consisting of bone or fibrocartilage, or membranous. In horses, the majority of affected cases are membranous • Choanal atresia is a relatively rare congenital craniofacial defect characterized by the obstruction of the posterior nasal passages. • The incidence rate has been noted to range between 1 in 5,000 and 1 in 10,000 live births The CHARGE association is a collection of multisystem congenital anomalies including choanal atresia. A review of the literature failed to identify any specific findings that suggested the need to alter the management of choanal atresia in these patients

  1. 1. Unilateral / Bilateral : Unilateral choanal atresia is an incidental finding and is verycommon (about 70%) 4. High degree of suspicion is necessary to identify this condition. An. infant with unilateral choanal atresia will have problems suckling milk from the breast opposite to the side of atresia. 2
  2. During the last decade, computed tomography (CT) has become the standard technique for diagnosing and assessing the condition of a neonate with choanal atresia because the abnormal bony and membranous deformities can be readily seen on CT images. 1-4 However, less has been published about the neonate with nasal obstruction but without choanal.
  3. Ramsden JD, Campisi P, Forte V. Choanal atresia and choanal stenosis. Otolaryngol Clin North Am. 2009 Apr;42(2):339-52; Syed I, Jephson C. Choanal atresia. Br J Hosp Med (Lond). 2012 Dec;73(12):687-90; Corrales CE, Koltai PJ. Choanal atresia: current concepts and controversies. Curr Opin Otolaryngol Head Neck Surg. 2009 Dec;17(6):466-7
  4. ed. CLINICAL FINDINGS: Endoscopy and computed tomography (CT) demonstrated a complete membranous obstruction of the left nasal choana, confir
  5. ation in order to obtain the maximum of information pre-operatively

DOI: 10.2307/30134302 Corpus ID: 80368466. Choanal atresia in an African grey parrot (Psittacus erithacus erithacus) and an umbrella cockatoo (Cacatua alba) @inproceedings{Greenacre1993ChoanalAI, title={Choanal atresia in an African grey parrot (Psittacus erithacus erithacus) and an umbrella cockatoo (Cacatua alba)}, author={C. Greenacre and E. Watson and B. Ritchie}, year={1993} Choanal atresia is a congenital disorder where the back of the nasal passage is blocked, usually by abnormal bony or soft tissue (membranous) due to failed recanalization of the nasal fossae during fetal development. It was first described by Roederer in 1755

Choanal atresia is a congenital condition involving occlusion of the posterior choanae in the nasal cavity by bone, soft tissue, or both. [1, 2] Complete nasal obstruction in a newborn may cause death from asphyxia.During attempted inspiration, the tongue is pulled to the palate, and obstruction of the oral airway results Bilateral Choanal Atresia is a more serious condition that requires emergency medical support and prompt treatment; Additional and Relevant Useful Information for Choanal Atresia: Studies have shown that Choanal Atresia is linked to a common herbicide (atrazine) used for treating crops in the US A 16-year-old female patient with recurrent stenosis after unilateral choanal atresia that had been treated by surgery and laser therapy presented with restenosis 3 weeks after laser resection. As an alternative to repeat surgery, she was treated by balloon dilatation. Four balloon dilatations were performed (three at 4-week intervals and the last after an 8-week interval) over a 4-month. * Unilateral choanal atresia can present later in child or adulthood as a unilateral blocked nostril, stuffiness and unilateral nasal discharge. Radiological diagnosis: - Previously the radiographic diagnosis was made by water soluble contrast being inserted into the nasal cavity and obtaining lateral horizontal beam views

Ontology: Choanal Atresia (C0008297) Definition (MSH) A congenital abnormality that is characterized by a blocked CHOANAE, the opening between the nose and the NASOPHARYNX. Blockage can be unilateral or bilateral; bony or membranous. Concepts Abstract: BACKGROUND:Bilateral choanal atresia in patients with CHARGE syndrome becomes symptomatic immediately after birth. A prompt diagnosis, the implementation of sufficient preliminary measures, and the delivery of surgical therapy are crucial. This article is intended to assist in terms of diagnostics and a therapy recommendation Choanal atresia - Wikipedia. The transnasal microsurgical repair with endonasal stent proved to be a safe and effective procedure. Are stents necessary after choanal atresia repair?. The most common congenital causes are choanal atresia CAdermoid cyst, glioma, encephalocele and congenital stenosis of the piriform aperture Choanal atresia: How useful is computed tomography. E E Dawlatly Departments of Otorhinolaryngology and Radiology, College of Medicine and Medical Sciences, King Fahd Hospital of the University, Al-Khobar, Saudi Arabia

Choanal atresia: precise CT evaluatio

Choanal Atresia Pediatric Radiology Reference Article

nal anomalies, airway management, and complications that arose in 41 patients with choanal atresia who were operated on between 2009 and 2016 were evaluated retrospectively by examining their medical and anaesthesia records. Results: The patients were divided into 2 groups: Group I—bilateral choanal atresia and Group II—unilateral choanal atresia. Of the 41 patients included in the study. OSTI.GOV Journal Article: Treatment of a Recurrent Choanal Atresia by Balloon Dilatatio

Unilateral choanal atresia presents late and can be asymptomatic or present with rhinorrhoea. Bilateral atresia can present with neonatal respiratory distress as infants are obligate nose breathers. Choanal atresia | Radiology Reference Article | Another finding is failure to pass a nasogastric tube Choanal atresia may affect one or both sides of the nasal airway. Choanal atresia blocking both sides of the nose causes acute breathing problems with bluish discoloration and breathing failure. Such infants may need resuscitation at delivery. More than one half of infants have a blockage on only one side, which causes less severe problems

Choanal atresia: a case report illustrating the use of

Choanal atresia. Choanal atresia is a rare condition that is present from birth, in which the nasal passages are blocked by bone or tissue. This condition can affect one or both nasal passages. This page explains about choanal atresia and what to expect when your child comes to Great Ormond Street Hospital (GOSH) for treatment ATRESIA DE LAS COANAS PDF. Choanal atresia (CA) is a relatively uncommon but well-recognized condition characterized by the anatomical closure of the posterior choanae. Choanal atresia refers to a lack of formation of the choanal openings. It can be unilateral or bilateral. Epidemiology It frequently presents in neonates where it is Choanal atresia (CA) occurs in roughly 1:5000-7000 live births. It affects females twice as often as males, and occurs bilaterally in roughly 50% of cases. Bilateral choanal atresia (BCA) is typically repaired in the newborn period as soon as the child is medically stable; tracheostomy for BCA alone has been widely abandoned. Unilateral CA repair is often deferred until age 2-3 years Radiology Radiotherapy <p>Choanal atresia is a rare cryptic congenital anomaly with developmental failure of the nasal cavity to communicate with the nasophaynx, resulting in a significant physiological and anatomical alteration of the dento-facial complex. It is considered as a life-threatening or lethal congenital malformation in an.

Choanal Atresia and Nasal Pyriform - Radiology Ke

sia. CT evaluation of suspected choanal atresia/stenosis confirms the diagnosis and helps plan surgery. Measurements of the structures outlined allows for an objective and reproducible set of criteria for the diagnosis of choanal atresia and stenosis. References 1. Slovis TLR. Choanal atresia: precise CT evaluation. Radiology 1985; 155: 345-348. 2 Index Terms: choanal atresia, girl, computed tomography, choanography. I. INTRODUCTION Choanal atresia is the developmental failure of the nasal cavity to communicate with the nasopharynx. 1. It is a rare malformation that causes airway obstruction in newborns and infants. It has an incidence of 1 in 50008000 live births. Females are more.

Choanal Atresia Children's Hospital of Philadelphi

In membranous choanal atresia, the buccopharyngeal membrane does not resorb. In most cases, there is a combination of boney and membranous types. Choanal atresia occurs in one of 8000 live births and is commonly associated with syndromes (eg, CHARGE, synostosis) . Approximately two-thirds of cases are bilateral Choanal atresia is a predominately bony occlusion of the posterior choanae (the posterior nasal cavity transition to the nasophayrnx). Unilateral choanal atresia presents with unilateral purulent rhinorrhea and a mild breathing obstruction. Patients with bilateral choanal atresia present with severe respiratory distress in the immediate newborn.

Choanal Atresia-CT - Sumer's Radiology Blo

Choanal atresia | Image | Radiopaedia

Choanal atresia Eurora

Choanal atresia (CA) is an obliteration or blockage of the posterior nasal aperture, limiting or obstructing the nasal airway to the nasopharynx. The presentation of unilateral CA commonly occurs at a later age than those children affected by bilateral CA (BCA) and can often persist undiagnosed into adulthood. BCA, on the other hand, typically presents with respiratory obstruction within the. Choanal atresia occurs as a fetus is growing in the womb. For reasons that are not entirely understood, the thin tissue that separates the mouth and nose does not separate which leads to an obstruction of airflow between the nose and throat. What are the symptoms of choanal atresia? Difficulty breathing, nasal discharge, a sunken chest and. Bilateral choanal atresia is a life threatening condition. CT scan plays an important role in diagnosing the nature & extent of the choanal atresia, to rule out other causes of congenital nasal obstruction and also helpful in therapeutic approach. The introduction of multidetector CT scanner offers several additional advantages Bilateral choanal atresia is a life-threatening condition and a well-recognized cause of airway obstruction and respiratory distress in the newborn. Lingual Thyroid or Thyroglossal Cyst. A lingual.

Choanal Atresia Workup: Imaging Studies, Diagnostic Procedure

CHARGE is a rare congenital anomaly syndrome, with ocular coloboma, congenital heart defects, choanal atresia, retardation of growth and development, genital hypoplasia and ear anomalies associated with deafness. The syndrome was first described in 1979 by B.D. Hall, as referenced by Blake and Prasad 1 More pediatric radiology resources at PediatricRadiology.com Pediatric Imaging is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License . Follow Pediatric Imaging via Emai

CHARGE syndrome is a congenital condition (present from birth) that affects many areas of the body. CHARGE stands for c oloboma, h eart defect, a tresia c hoanae (also known as choanal atresia), r estricted growth and development, g enital abnormality, and e ar abnormality. Signs and symptoms vary among people with this condition; however, infants often have multiple life-threatening medical. Pulmonary Embolism-Spiral CT. Pulmonary embolism (PE) was clinically described in the early 1800s, and von Virchow first described the connection between venous thrombosis and PE. This image shows an intraluminal filling defect that occludes the left pulmonary artery. Also present is an infarction of the corresponding lung, which is indicated. Choanal atresia (CA) is a life-threatening, but relatively uncommon, anomaly involving the congenital obliteration or narrowing of the posterior nasal choana, resulting due to the blocked oronasal membrane in children .The incidence of CA is one in 5-9000 live births .The nasal obstruction in CA can be either bony or membranous; while early reports suggested the bony and membranous obstruction. Congenital posterior choanal atresia is an uncommon anomaly which may have life-threatening consequences. This defect is frequently associated with other congenital abnormalities. CT scan confirms the diagnosis and accurately defines the anatomy of the atresia and differentiates osseous stenosis from membranous stenosis in the choanae

Endoscopic treatment of choanal atresi

Introduction. Truncus arteriosus (TA) is occasionally associated with right aortic arch (RAA) or aortic arch (AA) interruption, but very uncommonly with double aortic arch (DAA) (1,2).A previously unreported case of a child with an exceedingly rare amalgamation of complex defects, including TA, DAA, tracheoesophageal fistula (TEF), and choanal atresia (CA), managed with a staged, multi. Choanal Atresia and Upper Airway Abnormalities Approximately 65% of patients with CHARGE syndrome may have obstructed breathing due to choanal atresia at birth. [11] Other upper airway abnormalities that can be seen in CHARGE syndrome include: laryngomalacia, tracheomalacia, tracheoesophageal fistula, and subglottic stenosis

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Radiological Parameters Review for Choanal Atresi

Objective. To illustrate the role of multislice computed tomography and local contrast instillation in the diagnosis and characterization of choanal atresia. To review the common associated radiological findings. Methods. We analyzed 9 pediatric patients (5 males and 4 females) with suspected choanal atresia by multislice computed tomography 15 Mar 2012. no randomized or quasi-randomized trials identified evaluating surgery for congenital choanal atresia (Cochrane Database Syst Rev 2012 Feb 15

Choanal Atresia: How Useful Is Computed Tomography

Choanal atresia. Choanal atresia is a congenital (present at birth) occlusion of the back of the nasal cavity by bone, soft tissue, or both, due to failed recanalization of the nasal fossae during fetal development that causes difficulty breathing 1).Choanal atresia is rare, occurring in approximately 1 in 7,000 live births, and is seen more often in females than in males (females to males. Our evaluation of a female infant with multiple anomalies including absence of the sella turcica, a normal pituitary in the craniopharyngeal canal, normal pituitary function, choanal atresia and anomalies of the appendiceal skeleton prompted a review of the occurrence and biology of an absent sella turcica. KW - Adenohypophysis. KW - Choanal. Choanal atresia (CA) is a relatively uncommon but well-recognized condition characterized by the anatomical closure of the posterior choanae. Choanal atresia refers to a lack of formation of the choanal openings. It can be unilateral or bilateral. Epidemiology It frequently presents in neonates where it is . Choanal atresia DuPage Children's ENT & Allergy. 1331 W 75th Street Naperville, IL 60540-931 These categories comprise anomalies that are related to the nasal cavity, nasofrontal region, nasolacrimal apparatus, and craniofacial syndromes. CT is the imaging modality of choice in children with possible choanal atresia, pyriform aperture stenosis, or anomalies of the nasolacrimal duct (eg, nasolacrimal duct stenosis, dacryocystoceles)

Choanal atresia; Atresia, Choanal

CT - Choanal Atresi

Bosma arhinia microphthalmia syndrome (BAMS) is a rare condition characterized by abnormalities of the nose and eyes and problems with puberty.. The key feature of BAMS is arhinia, which is the absence of an external nose. While most people with BAMS are born without a nose, some affected individuals have a severely underdeveloped (hypoplastic) nose Solitary median maxillary central incisor (SMMCI) is a rare dental anomaly. It is estimated to occur in 1 : 50,000 live births. The SMMCI tooth differs from the normal central incisor in that the crown form is symmetric and it develops and erupts precisely in the midline of the maxillary dental arch in both primary and permanent dentitions The atresia can be membranous or bony in nature, but is usually mixed in most cases. When the atresia is bilateral, newborns can have severe airway distress and cyanosis is alleviated by crying. Bilateral choanal atresia is managed with an oropharyngeal airway. Flexible nasal endoscopy and computed tomography can confirm the diagnosis

Roentgen Ray Reader: Choanal Atresi

The topic Craniosynostosis, Choanal Atresia, Radial Humeral Synostosis you are seeking is a synonym, or alternative name, or is closely related to the medical condition Antley-Bixler Syndrome. Quick Summary: Antley-Bixler Syndrome (ABS) is a very rare disorder resulting from the presence of abnormal genes in the human genome Intestinal malrotation and midgut volvulus / Grace S. Phillips --Duodenal atresia and duodenal stenosis / C. Anne Waugh Moore --Jejunal atresia / Charles Mason Maxfield --Distal bowel obstruction in the newborn / Caroline Carrico --Meconium peritonitis / Charles Mason Maxfield --Necrotizing enterocolitis / Beverly P. Wood --Esophageal atresia.