| Literature DB >> 11045594 |
A Mégarbané, I Melki, N Souraty, J Gerbaka, V El Ghouzzi, J Bonaventure, A Mornand, J Loiselet.
Abstract
We report a male patient with craniosysnostosis, bilateral radial and ulnar hypoplasia, absent thumbs, poikiloderma, and short stature. His parents are first cousins. Although this patient was originally diagnosed as having Baller-Gerold syndrome it is more likely that he has Rothmund-Thomson syndrome or a similar disorder. This report confirms the overlap between these two syndromes, and that Baller-Gerold syndrome is essentially a diagnosis of exclusion.Entities:
Mesh:
Year: 2000 PMID: 11045594 DOI: 10.1097/00019605-200009040-00018
Source DB: PubMed Journal: Clin Dysmorphol ISSN: 0962-8827 Impact factor: 0.816