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Recurrence of diaphragmatic agenesis associated with multiple midline defects: evidence for an autosomal gene
L M Bird1, R O Newbury, R Ruiz-Velasco
1Division of Genetics, Children's Hospital and Health Center, San Diego, California 92123.
American Journal of Medical Genetics
|October 15, 1994
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.