A Turkish case of subcortical/subependymal heterotopia associated with corpus callosum dysgenesis, craniofacial dysmorphism, severe eye abnormalities, and growth-mental retardation

Genetic Counseling

Volumn 14, Issue 3, 2003, Pages 343-348

  Çaksen, Hüseyin ^a,c   Tuncer, O ^a   Atasl B ^a   Demirok, A ^a   Ünal, Ö ^a   Ikbal, M ^b   Odabas D ^a  

^a YUZUNCU YIL UNIVERSITY   (Turkey)

^b ATATURK UNIVERSITY   (Turkey)

^c NONE   (Turkey)

Author keywords

Corpus callosum dysgenesis; Craniofacial dysmorphism; Eye abnormality; Heterotopia

Indexed keywords

ARTICLE; BODY HEIGHT; BODY WEIGHT; BRAIN MALFORMATION; CAFE AU LAIT SPOT; CASE REPORT; CHROMOSOME ANALYSIS; CLINICAL FEATURE; COLOBOMA; CONVERGENT STRABISMUS; CORPUS CALLOSUM DYSGENESIS; CRANIOFACIAL MALFORMATION; DISEASE ASSOCIATION; EYE MALFORMATION; FACE ASYMMETRY; FRONTAL LOBE; FRONTAL SINUS; FUNNEL CHEST; GLAUCOMA; GRANULATION TISSUE; GROWTH RETARDATION; HEAD CIRCUMFERENCE; HETEROTOPIA; HUMAN; INTELLIGENCE QUOTIENT; KARYOTYPE 46,XY; LEARNING DISORDER; MALE; MENTAL DEFICIENCY; NUCLEAR MAGNETIC RESONANCE IMAGING; NYSTAGMUS; OPHTHALMOSCOPY; OPTIC NERVE ATROPHY; SCHOOL CHILD; SLOW BRAIN WAVE; VISUAL ACUITY;

ABNORMALITIES, MULTIPLE; BRAIN DISEASES; CHILD; CHORISTOMA; CORPUS CALLOSUM; EYE ABNORMALITIES; GROWTH DISORDERS; HUMANS; KARYOTYPING; MAGNETIC RESONANCE IMAGING; MALE; MENTAL RETARDATION; SKULL;

EID: 0141532985     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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