Two Cases of Congenital Hypothalamic Hamartoblastoma, Polydactyly, and Other Congenital Anomalies (Pallister-Hall Syndrome)
- 18 February 1982
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 306 (7), 430-431
- https://doi.org/10.1056/nejm198202183060719
Abstract
To the Editor: Haas,1 Hall,2 and Clarren3 and their colleagues have described a curious group of six infants, each with a hypothalamic hamartoblastoma (a very rare tumorous malformation) and a remarkably similar array of associated malformations, hamartomas, and dysplasias. Recently, two infant boys with similar syndromes were studied by autopsy at St. Christopher's Hospital for Children in Philadelphia. The infants were born eight days apart in early April. Their dates of death were eight weeks apart.The first boy was born at 35 weeks' gestation. The mother had used marijuana, cocaine, and methaqualone (Quaalude) during early pregnancy. Respiratory distress, seizures, . . .This publication has 2 references indexed in Scilit:
- Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly—a new syndrome? Part I: Clinical, causal, and pathogenetic considerationsAmerican Journal of Medical Genetics, 1980
- Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly—a new syndrome? Part II: Neuropathological considerationsAmerican Journal of Medical Genetics, 1980