Further delineation of the Beemer–Langer syndrome using concordance rates in affected sibs
- 1 May 1994
- journal article
- review article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 50 (4) , 313-317
- https://doi.org/10.1002/ajmg.1320500403
Abstract
Six familial cases of the Beemer–Langer syndrome (BLS) were analyzed to further elucidate the spectrum and frequency of anomalies observed in this disorder. Preaxial polydactyly was found in 3/6 affected sibs, and, therefore, its frequency previously may have been underestimated. Some patients, described as infants affected with the Majewski syndrome (MS) or “atypical” short rib‐poly‐dactyly conditions, may indeed have BLS. A high frequency of brain defects (16/26) and cleft tongue, oral frenula, and/or natal teeth (13/29) widens the list of typical findings in this syndrome. The specific type of tibial defect seems to be the most important discrimination of the MS and the BLS.Keywords
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