Blepharophimosis sequence and diaphragmatic hernia associated with interstitial deletion of chromosome 3 (46,XY,del(3)(q21q23)).

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منابع مشابه

Blepharophimosis sequence and diaphragmatic hernia associated with interstitial deletion of chromosome 3 (46,XY,del(3)(q21q23)).

A case of blepharophimosis, ptosis, and epicanthus inversus (BPES) associated with prenatally diagnosed diaphragmatic hernia and interstitial deletion of the long arm of chromosome 3, del(3)(q21q23), is reported. Comparison with other cases of BPES resulting from 3q rearrangements indicate that this disorder, previously assigned to 3q2, can now be more accurately mapped to 3q23.

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We report a case of an infant with congenital diaphragmatic hernia (CDH) and hydrops fetalis who died from hypoxic respiratory failure. Autopsy revealed type B interrupted aortic arch (IAA). Microarray revealed a female karyotype with deletion of chromosome 1p21.1p12. There may be an association between 1p microdeletion, CDH, and IAA.

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Anesthesie et Reanimation pour Hemie diaphragmatique du Nouveau -ne. Le diagnostic de la hernie diaphragrnatique du nouveau -ne se fait tres tot et souvent dans lasallle d'accouchement. La compression et le deplacemen t des or­gan es thoraciques ainsi que les gros vais­seaux du rnediastin provoquent rapidernent une insuffisance cardio respiratoire aigue. La chirurgie est indiquee desque le diag...

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ژورنال

عنوان ژورنال: Journal of Medical Genetics

سال: 1994

ISSN: 1468-6244

DOI: 10.1136/jmg.31.8.647