Semilobar holoprosencephaly in Seckel syndrome.
Indian J Pediatr
;
2008 May; 75(5): 519-20
Article
in English
| IMSEAR
| ID: sea-83251
ABSTRACT
Seckel syndrome is a rare genetic disorder with autosomal recessive inheritance. It is associated with many CNS anomalies along with involvement of other systems. We present a case of Seckel syndrome with semilobar holoprosencephaly as associated CNS anomaly, which to the best of our knowledge has not been reported earlier.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Syndrome
/
Abnormalities, Multiple
/
Humans
/
Male
/
Infant, Newborn
/
Holoprosencephaly
/
Dwarfism
/
Intellectual Disability
/
Microcephaly
Language:
English
Journal:
Indian J Pediatr
Year:
2008
Type:
Article
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