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{{SK}} Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency.
{{SK}} Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency.
==Overview==
==Overview==
Braddock syndrome is characterised by the association of VACTERL-like defects, pulmonary hypertension, abnormal ears, blue sclerae, laryngeal webs, and persistent growth deficiency. Patients show normal intellect, no tracheo-oesophageal fistula, and no anal atresia. This new syndrome has been described in one sibship. Inheritance is probably autosomal recessive. Vital prognosis depends on cardiac and pulmonary function.<ref>http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=10685&Disease_Disease_Search_diseaseType=ORPHA&Disease_Disease_Search_diseaseGroup=52047&Maladie%28s%29/groupes%20de%20maladies=Syndrome-de-Vater-like---hypertension-pulmonaire---anomalies-des-oreilles---retard-de-croissance&title=Syndrome-de-Vater-like---hypertension-pulmonaire---anomalies-des-oreilles---retard-de-croissance&search=Disease_Search_Simple</ref>
Braddock syndrome is characterised by the association of [[VACTERL]]-like defects, [[pulmonary hypertension]], [[abnormal ears]], [[blue sclerae]], [[laryngeal webs]], and persistent growth deficiency. Patients show normal intellect, no [[tracheo-oesophageal fistula]], and no [[anal atresia]]. This new syndrome has been described in one sibship. Inheritance is probably [[autosomal recessive]]. Vital prognosis depends on cardiac and pulmonary function.<ref>http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=10685&Disease_Disease_Search_diseaseType=ORPHA&Disease_Disease_Search_diseaseGroup=52047&Maladie%28s%29/groupes%20de%20maladies=Syndrome-de-Vater-like---hypertension-pulmonaire---anomalies-des-oreilles---retard-de-croissance&title=Syndrome-de-Vater-like---hypertension-pulmonaire---anomalies-des-oreilles---retard-de-croissance&search=Disease_Search_Simple</ref>


==References==
==References==
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Latest revision as of 12:25, 5 October 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency.

Overview

Braddock syndrome is characterised by the association of VACTERL-like defects, pulmonary hypertension, abnormal ears, blue sclerae, laryngeal webs, and persistent growth deficiency. Patients show normal intellect, no tracheo-oesophageal fistula, and no anal atresia. This new syndrome has been described in one sibship. Inheritance is probably autosomal recessive. Vital prognosis depends on cardiac and pulmonary function.[1]

References

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