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mandibuloacral dysplasia type A lipodystrophy
Summary
- Definition
- A mandibuloacral dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding lamin A/C (LMNA) on chromosome 1q22 and that is characterized by growth retardation, craniofacial anomalies with mandibular hypoplasia, skeletal abnormalities with progressive osteolysis of the distal phalanges and clavicles, and pigmentary skin changes. The lipodystrophy is characterized by a marked acral loss of fatty tissue with normal or increased fatty tissue in the neck and trunk.
- Super Class
- mandibuloacral dysplasia
External Links
- Disease Ontology
- DOID:0081128
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
