A Case of Cerebral Dystrophy and Cerebellar Atropy in Seckel Syndrome
Journal of the Korean Child Neurology Society
;
: 121-125, 2007.
Article
in Korean
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Atrophy
/
Beak
/
Nose
/
Head
/
Intellectual Disability
/
Microcephaly
Limits:
Animals
/
Humans
Language:
Korean
Journal:
Journal of the Korean Child Neurology Society
Year:
2007
Type:
Article
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