Abstract
Neu-Laxova syndrome is a rare congenital disorder characterized by microcephaly, limb contactures, lissencephaly and ichthyosis. A case of Neu-Laxova syndrome is presented, with a discussion of clinical manifestations, complications, and therapeutic interventions.
MeSH terms
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Abnormalities, Multiple / diagnosis*
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Abnormalities, Multiple / therapy
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Brain / abnormalities*
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Disease Progression
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Fatal Outcome
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Humans
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Ichthyosis / complications
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Ichthyosis / diagnosis*
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Infant, Newborn
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Limb Deformities, Congenital / complications
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Limb Deformities, Congenital / diagnosis*
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Male
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Microcephaly / complications
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Microcephaly / diagnosis
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Rare Diseases
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Risk Assessment
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Syndrome