Spectrum of the acrocallosal syndrome

American Journal of Medical Genetics

Volumn 108, Issue 1, 2002, Pages 7-11

  Koenig, Rainer ^a,c   Bach, Alexia ^a   Woelki, Ulrike ^a   Grzeschik, Karl Heinz ^b   Fuchs, Sigrun ^a  

^a GOETHE UNIVERSITY   (Germany)

^b PHILIPPS UNIVERSITY MARBURG   (Germany)

^c Institut fur Humangenetik   (Germany)

Author keywords

Acrocallosal syndrome; Agenesis corpus callosum; Arachnoid cyst; Postaxial polydactyly; Preaxial polydactyly

Indexed keywords

ACROCALLOSAL SYNDROME; ARTICLE; BRAIN ARACHNOID CYST; CASE REPORT; CHILD; CLINICAL EXAMINATION; CORPUS CALLOSUM AGENESIS; DIFFERENTIAL DIAGNOSIS; FOOT RADIOGRAPHY; HUMAN; INFANT; MALE; MALFORMATION SYNDROME; NUCLEAR MAGNETIC RESONANCE IMAGING; POLYDACTYLY; PRIORITY JOURNAL; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; ARACHNOID CYSTS; CHILD, PRESCHOOL; CORPUS CALLOSUM; CRANIOFACIAL ABNORMALITIES; HUMANS; INFANT; INFANT, NEWBORN; MAGNETIC RESONANCE IMAGING; MENTAL RETARDATION; PHENOTYPE; POLYDACTYLY; PSYCHOMOTOR DISORDERS; SYNDROME;

ARACHNOIDEA;

EID: 0037082969     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10236     Document Type: Article

References (19)

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4. Acrocallosal syndrome in an Algerian boy born to consanguineous parents: Review of the literature and further delineation of the syndrome
5. The variable clinical spectrum and mental prognosis of the acrocallosal syndrome
6. Polysyndactyly and trigonocephaly with partial agenesis of the corpus callosum: An example of the variable clinical spectrum of the acrocallosal syndrome?
7. Further delineation of the acrocallosal syndrome
8. Acrocallosal syndrome: Report of a Brazilian girl
9. Acrocallosal syndrome
10. Recurrent anencephaly as a primary manifestation of the acrocallosal syndrome
11. The acrocallosal syndrome: Expansion of the phenotypic spectrum
12. Acrocallosal syndrome: New findings
13. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3
14. Acrocallosal syndrome in a girl born to consanguineous parents
15. Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macroencephaly and severe mental retardation: A new syndrome?
16. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation and additional anomalies in two unrelated patients: A new syndrome
17. Fronto-nasal dysostosis, callosal agenesis, crossed-fused ectopia, tibial hemimelia, and preaxial polydactyly of feet: Severe expression of the acrocallosal syndrome?
18. Acrocallosal syndrome: Association with cystic malformation of the brain and neurodevelopmental aspects
19. GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families