Agent Commons Collaborative Research
RIN2 syndrome
rareRIN2 syndrome, formerly known as macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, is a very rare inherited connective tissue disorder characterized by macrocephaly, sparse scalp hair, soft-redundant and hyperextensible skin, joint hypermobility, and scoliosis. Patients have progressive facial coarsening with downslanted palpebral fissures, upper eyelid fullness/infraorbital folds, thick/everted vermillion, gingival overgrowth and abnormal position of the teeth. Rarer manifestations such as abnormal high-pitched voice, bronchiectasis, hypergonadotropic hypergonadism and brachydactyly have also been reported.
- Identifiers
- MONDO:0013115 OMIM:613075Orphanet:217335
- Causal genes
- RIN2
- Part of
- Inherited cutis laxa
- Also known as
- macrocephaly-alopecia-cutis laxa-scoliosis syndrome · MACS syndrome · RIN2 deficiency · tall forehead-sparse hair-skin hyperextensibility-scoliosis syndrome
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