Autosomal dominant isolated ('uncomplicated') microcephaly.
- 1 November 1988
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 25 (11) , 750-753
- https://doi.org/10.1136/jmg.25.11.750
Abstract
A large family (13 affected members in three generations) is reported in which isolated microcephaly occurred without any other dysmorphic or neurological abnormalities. The family pedigree confirms the autosomal dominant mode of inheritance with incomplete penetrance, including one example of male to male transmission and the occurence of a non-manifesting heterozygote resulting in a ''skipped generation''. There is considerable variation in the phenotypic expression of autosomal dominant microcephaly. This isolated (uncomplicated)type of microcephaly should be distinguished from other well defined, dominantly inherited forms of microcephaly.This publication has 14 references indexed in Scilit:
- Dominantly inherited syndrome of microcephaly and congenital lymphedemaClinical Genetics, 1985
- Anthropometric measurements of the newborn infant (27 to 41 gestational weeks).1984
- Silent microcephaly: A distinct autosomal dominant traitClinical Genetics, 1983
- Chorio‐retinal dysplasia, microcephaly and mental retardation. An autosomal dominant syndromeClinical Genetics, 1981
- Dominant inheritance of microcephaly with short statureClinical Genetics, 1981
- Little heads: Inheritance and early detectionThe Journal of Pediatrics, 1979
- Autosomal dominant microcephalyThe Journal of Pediatrics, 1979
- Intrauterine growth of live-born Caucasian infants at sea level: Standards obtained from measurements in 7 dimensions of infants born between 25 and 44 weeksPublished by Elsevier ,1969
- Head circumference from birth to eighteen years. Practical composite international and interracial graphs.1968
- A clinical and genetical study of microcephaly.1953