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Neu-Laxova syndrome
rareNeu-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.
- Identifiers
- MONDO:0000179 Orphanet:2671
- Part of
- 3-phosphoglycerate dehydrogenase deficiencyDevelopmental anomaly of metabolic originIntegumentary system disorderLissencephaly type 3Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilitySyndromic disease
- Also known as
- Neu Laxova syndrome · NLS
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.