Neu-Laxova syndrome

MONDO:0000179

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.

Also known as: NLS, Neu Laxova syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Neu-Laxova syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Syndromic disease (7133) ↑ Integumentary system disorder (4553) ↑ Developmental anomaly of metabolic origin (383) ↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ 3-phosphoglycerate dehydrogenase deficiency (1) ↑ Lissencephaly type 3 (0)

Sub-types of Neu-Laxova syndrome

Neu-Laxova syndrome 1 0 trials
Neu-Laxova syndrome 2 0 trials
Neu-laxova syndrome due to 3-phosphoserine phosphatase deficiency 0 trials

Including sub-types (0) Tagged with Neu-Laxova syndrome (0)

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