FG syndrome in a premature male
- 1 October 1984
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 19 (2), 383-386
- https://doi.org/10.1002/ajmg.1320190221
Abstract
A 30‐week premature male infant is presented with dolichocephaly, frontal bossing, down‐slanting palpebral fissures, hypertelorism, long philtrum, micrognathia, cleft palate, and imperforate anus. He is the fifth patient to be presented with FG syndrome and sensorineural deafness. The patient's syndromic manifestations became more obvious during an inpatient observation period of 3 months.Keywords
This publication has 4 references indexed in Scilit:
- Sensorineural deafness in the FG syndrome: Report on four new casesAmerican Journal of Medical Genetics, 1984
- Studies of malformation syndromes of humans XXXIIIC: The FG syndrome — further studies on three affected individuals from the FG familyAmerican Journal of Medical Genetics, 1982
- The FG syndrome: Further characterization, report of a third family, and of a sporadic caseAmerican Journal of Medical Genetics, 1977
- Studies of malformation syndromes of man XXXIII: The FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardationEuropean Journal of Pediatrics, 1974