Severe Renal Dysgenesis Produced by a Dominant Gene
- 1 December 1976
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Pediatrics & Adolescent Medicine
- Vol. 130 (12) , 1356-1357
- https://doi.org/10.1001/archpedi.1976.02120130062012
Abstract
• A woman with the autosomal dominant syndrome of preauricular pits, cervical fistulae, and partial deafness gave birth to two children with preauricular pits and severe renal dysgenesis. The facies had some features of the Potter facies of renal agenesis. One child died soon after birth because of pneumothorax and immature development of the lungs. We suggest that all infants with renal agenesis or dysgenesis be examined for preauricular pits because of the high recurrence risk of renal anomalies in families with this syndrome. (Am J Dis Child 130:1356-1357, 1976)This publication has 4 references indexed in Scilit:
- The Temporal Bone in the Preauricular Pit, Cervical Fistula, Hearing Loss SyndromeAnnals of Otology, Rhinology & Laryngology, 1976
- Oligohydramnios: Further commentThe Journal of Pediatrics, 1974
- Lateral Cervical and Preauricular Sinuses: Their Transmission as Dominant CharactersBMJ, 1961
- Bilateral renal agenesisThe Journal of Pediatrics, 1946