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Simpson-Golabi-Behmel syndrome types I and II
Simpson-Golabi-Behmel syndrome (SGBS) is a rare overgrowth syndrome clinically characterized by multiple congenital abnormalities, pre/postnatal overgrowth, distinctive craniofacial features, macrocephaly, and organomegaly. Abnormalities of the skeletal system, heart, central nervous system, kidney,...
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| Foilsithe in: | Orphanet J Rare Dis |
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| Main Authors: | , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BioMed Central
2014
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4254265/ https://ncbi.nlm.nih.gov/pubmed/25238977 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-014-0138-0 |
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