A new X‐linked multiple congenital anomalies/ mental retardation syndrome
- 1 January 1984
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 17 (1) , 367-374
- https://doi.org/10.1002/ajmg.1320170130
Abstract
We report on 2 boys, the sons of sisters, and their mother's brother who have a new, X‐linked multiple congenital anomalies/mental retardation (MCA/MR) syndrome. The propositus was a 16‐month‐old caucasian male with 1)mental retardation, 2) congenital microcephaly, 3)postnatal growth deficiency, 4)ridged metopic suture with narrow bifrontal diameter, 5)upslanted palpebral fissures with persistent epicanthal folds, strabismus, and lacrimal duct obstruction, 6)narrow palate, 7)macrodontia, 8)anteverted ears, 9)atrial septal defect, 10)dry brittle scalp hair and 11)cutis marmorata. His chromosomes were normal. His cousin and uncle were similarly affected. This distinctive MCA/MR syndrome is added to the list of X‐linked malformation syndromes known at the present time.Keywords
This publication has 6 references indexed in Scilit:
- X-linked mental retardation, macro-orchidism, and the Xq27 fragile siteThe Journal of Pediatrics, 1980
- X-linked mental retardation associated with macro-orchidism.Journal of Medical Genetics, 1975
- X-linked mental retardation without physical abnormality (Renpenning's syndrome) in sibs in an institution.Journal of Medical Genetics, 1972
- X‐linked Mental Retardation Without Physical Abnormality: Renpenning's SyndromeDevelopmental Medicine and Child Neurology, 1971
- RENPENNING'S SYNDROME—X-LINKED MENTAL RETARDATIONThe Lancet, 1970
- X-linked mental retardation. Study of a large kindred with 20 affected membersThe Journal of Pediatrics, 1965