Literature DB >> 7802033

Recurrence of diaphragmatic agenesis associated with multiple midline defects: evidence for an autosomal gene regulating the midline.

L M Bird1, R O Newbury, R Ruiz-Velasco, M C Jones.   

Abstract

We report the familial occurrence of diaphragmatic agenesis in association with other midline anomalies in a brother and sister. Opitz and Gilbert [Am J Med Genet 1982, 12:443-455] introduced the concept of the midline as a developmental field, and there have been reports of pedigrees compatible with the hypothesis of an X-linked gene regulating the development of the midline. This family suggests that an autosomal gene also contributes to the morphogenesis of midline structures.

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Year:  1994        PMID: 7802033     DOI: 10.1002/ajmg.1320530108

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  A newborn with very rare von Voss-Cherstvoy syndrome: a case report.

Authors:  Deepak Sharma; Basudev Gupta; Sweta Shastri; Pradeep Sharma
Journal:  Int Med Case Rep J       Date:  2016-07-20
  1 in total

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