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Up to: Syndromic disease · Integumentary system disorder · Developmental anomaly of metabolic origin · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · 3-phosphoglycerate dehydrogenase deficiency · Lissencephaly type 3

Neu-Laxova syndrome

Neu-Laxova syndrome (NLS) is a rare, multiple malformation syndrome characterized by severe intrauterine growth retardation (IUGR), severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism.

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