A Case of Cerebral Dystrophy and Cerebellar Atropy in Seckel Syndrome / 대한소아신경학회지
Journal of the Korean Child Neurology Society
;
(4): 121-125, 2007.
Artigo
em Coreano
| WPRIM
| ID: wpr-128283
ABSTRACT
Seckel syndrome is a rare autosomal recessive disease. The characteristic features of Seckel syndrome include Intrauterine and postnatal growth deficiency, severe microcephaly, and a bird-like head. General appearance of our patient was characterized by Pre- and postnatal growth retardation, microcephaly, large eye, and a beaked nose. The patient had mental retardation with CNS anomalies. The CNS anomalies seen in the patient included cerebral dysgenesis and cerebellar atrophy. So, we report the case of CNS anomalies in Seckel syndrome.
Texto completo:
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Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Atrofia
/
Bico
/
Nariz
/
Cabeça
/
Deficiência Intelectual
/
Microcefalia
Limite:
Animais
/
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Child Neurology Society
Ano de publicação:
2007
Tipo de documento:
Artigo
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