CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly [7]

American Journal of Medical Genetics

Volumn 136 A, Issue 4, 2005, Pages 357-

  Polizzi, A ^b   Pavone, P ^b   Iannetti, P ^c   Gambardella, A ^d   Ruggieri, M ^a  

^a INSTITUTE OF NEUROLOGICAL SCIENCES   (Italy)

^b UNIVERSITY OF CATANIA   (Italy)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

^d UNIVERSITY MAGNA GRAECIA OF CATANZARO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

FOLLITROPIN; GROWTH HORMONE; LUTEINIZING HORMONE; TERATOGENIC AGENT;

AUTISM; BRAIN DYSFUNCTION; BRAIN MALFORMATION; CASE REPORT; CENTRAL NERVOUS SYSTEM DISEASE; CLINICAL FEATURE; DIABETES INSIPIDUS; GENE MUTATION; GROWTH HORMONE DEFICIENCY; HEMANGIOMA; HOLOPROSENCEPHALY; HUMAN; HYPOGLYCEMIA; HYPOTHALAMIC PITUITARY DYSFUNCTION; INTELLIGENCE QUOTIENT; LANGUAGE DISABILITY; LETTER; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTIC NERVE DISEASE; OPTIC NERVE DYSPLASIA; OPTIC NERVE HYPOPLASIA; PRENATAL EXPOSURE; PRESCHOOL CHILD; PRIORITY JOURNAL; SEIZURE; SEPTOOPTIC DYSPLASIA; SOCIAL DISABILITY;

ABNORMALITIES, MULTIPLE; ADOLESCENT; AUTISTIC DISORDER; CENTRAL NERVOUS SYSTEM; CHILD, PRESCHOOL; HOLOPROSENCEPHALY; HUMANS; LANGUAGE DEVELOPMENT DISORDERS; MAGNETIC RESONANCE IMAGING; SEPTO-OPTIC DYSPLASIA;

EID: 23044486340     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30630     Document Type: Letter

References (7)

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