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J Korean Child Neurol Soc. 2007 May;15(1):121-125. Korean. Case Report.
Yoon JW , Lim JW , Cheon EJ , Ko KO , Lee YH .
Department of Pediatrics, College of Medicine, Konyang University, Daejeon, Korea.

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.

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