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Achondrogenesis type IB
rareAchondrogenesis type 1B (ACG1B), a form of achondrogenesis, is a rare lethal skeletal dysplasia characterized by severe micromelia with very short fingers and toes, a flat face, a short neck, thickened soft tissue around the neck, hypoplasia of the thorax, protuberant abdomen, a hydropic fetal appearance and distinctive histological features of the cartilage.
- Identifiers
- MONDO:0010966 OMIM:600972Orphanet:93298
- Part of
- SLC26A2-related skeletal dysplasiaAchondrogenesisInborn errors of metabolismMineral metabolism disease
- Also known as
- ACG1B · achondrogenesis Ib · achondrogenesis, Parenti-Fraccaro type · achondrogenesis, type IB · Fraccaro achondrogenesis
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