Hirschsprung disease, unusual face, mental retardation, epilepsy, and congenital heart disease: Goldberg-Shprintzen syndrome
- 31 December 1993
- journal article
- case report
- Published by Elsevier BV in Pediatric Neurology
- Vol. 9 (6), 479-481
- https://doi.org/10.1016/0887-8994(93)90029-c
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- The syndrome of hirschsprung disease, microcephaly, unusual face, and mental retardationAmerican Journal of Medical Genetics, 1990
- Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migration.Journal of Medical Genetics, 1988
- Smith‐Lemli‐Opitz syndrome‐type II: Multiple congenital anomalies with male pseudohermaphroditism and frequent early lethalityAmerican Journal of Medical Genetics, 1987
- The association of Waardenburg syndrome and Hirschsprung megacolonAmerican Journal of Medical Genetics, 1979