Dominantly inherited microcephaly, short stature and normal intelligence. 1992

R C Hennekam, and A van Rhijn, and F A Hennekam
Clinical Genetics Center, Utrecht, The Netherlands.

A large family is reported in which microcephaly and short stature is segregating as a probably autosomal dominantly inherited trait. Some affected members also show a delayed onset of puberty. No other clinical or radiological symptoms are present, and psychomotor development is normal. This short report confirms an earlier description of a similar family by Burton in 1981.

UI MeSH Term Description Entries
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D007360 Intelligence The ability to learn and to deal with new situations and to deal effectively with tasks involving abstractions.
D008831 Microcephaly A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.) Microlissencephaly,Severe Congenital Microcephaly,Congenital Microcephalies, Severe,Congenital Microcephaly, Severe,Microcephalies,Microcephalies, Severe Congenital,Microcephaly, Severe Congenital,Microlissencephalies,Severe Congenital Microcephalies
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D001827 Body Height The distance from the sole to the crown of the head with body standing on a flat surface and fully extended. Body Heights,Height, Body,Heights, Body
D005260 Female Females
D005799 Genes, Dominant Genes that influence the PHENOTYPE both in the homozygous and the heterozygous state. Conditions, Dominant Genetic,Dominant Genetic Conditions,Genetic Conditions, Dominant,Condition, Dominant Genetic,Dominant Gene,Dominant Genes,Dominant Genetic Condition,Gene, Dominant,Genetic Condition, Dominant
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

R C Hennekam, and A van Rhijn, and F A Hennekam
March 1991, Clinical genetics,
R C Hennekam, and A van Rhijn, and F A Hennekam
January 1987, American journal of medical genetics,
R C Hennekam, and A van Rhijn, and F A Hennekam
July 1970, The Journal of pediatrics,
R C Hennekam, and A van Rhijn, and F A Hennekam
May 1983, American journal of medical genetics,
R C Hennekam, and A van Rhijn, and F A Hennekam
June 1985, Clinical genetics,
R C Hennekam, and A van Rhijn, and F A Hennekam
November 1982, Oral surgery, oral medicine, and oral pathology,
R C Hennekam, and A van Rhijn, and F A Hennekam
November 1973, Helvetica paediatrica acta,
R C Hennekam, and A van Rhijn, and F A Hennekam
September 1971, The Journal of pediatrics,
R C Hennekam, and A van Rhijn, and F A Hennekam
August 1993, The American journal of pediatric hematology/oncology,
Copied contents to your clipboard!