An additional manifestation in acrocallosal syndrome: Temporal lobe hypoplasia

Genetic Counseling

Volumn 19, Issue 2, 2008, Pages 237-240

  Aykut, A ^a   Cogulu, Osgur ^a   Ekmekci, A Y ^a   Ozkinay, F ^a  

^a EGE UNIVERSITY   (Turkey)

Author keywords

Acrocallosal syndrome; Temporal lobe hypoplasia

Indexed keywords

ACROCALLOSAL SYNDROME; ARTICLE; BRAIN ATROPHY; CASE REPORT; CORPUS CALLOSUM AGENESIS; CRANIOFACIAL MALFORMATION; FEMALE; HUMAN; HYPOPLASIA; INFANT; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTIC NERVE ATROPHY; POLYDACTYLY; TEMPORAL LOBE HYPOPLASIA;

ABNORMALITIES, MULTIPLE; CORPUS CALLOSUM; FEMALE; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MENTAL RETARDATION; POLYDACTYLY; SYNDROME; TEMPORAL LOBE; TURKEY;

EID: 46949109180     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. CASAMASSIMA A.C., BENECK D., GEWITZ M.H., HOROWITZ M.A., WOOLF P.K., PETTERSEN I.M., SHAPIRO L.R.: Acrocallosal syndrome: additional manifestations. Am. J. Med. Genet., 1989, 32, 311-317.
2. FRYNS J.P., DEVRIENDT K., LEGIUS E.: Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum: an example of the variable clinical spectrum of the Acrocallosal syndrome? Clin. Dysmorphol., 1997, 6, 285-286.
3. MOESCHLER J.B., POBER B.R., HOLMES L.B., GRAHAM J.M.: Acrocallosal syndrome: new findings. Am. J. Med. Genet, 1989, 32, 306-310.
4. ONLINE MENDELIAN INHERITANCE IN MAN, OMIM (TM): Johns Hopkins University, Baltimore, MD. MIM Number: {200990}: {6/2/2004}: World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim/
5. SALGADO L.J., ALI C.A., CASTILLA E.E.: Acrocallosal syndrome in a girl born to consanguineous parents. Am. J. Med. Genet., 1989, 32, 298-300.