| Literature DB >> 6782211 |
P Balestrazzi, L Corrini, G Villani, M P Bolla, F Casa, S Bernasconi.
Abstract
This report concerns two new cases of the Cohen syndrome and gives further information on the variable phenotypical pattern of the disease. The frequency of major and minor clinical signs is reviewed from all the published reports. Among the minor signs we found previously undescribed skeletal abnormalities in one of our patients. The reported delay onset of puberty, which appears to be a frequent aspect of the syndrome, seems to occur without LH and FSH deficiency, as our patients show.Entities:
Mesh:
Substances:
Year: 1980 PMID: 6782211 PMCID: PMC1885916 DOI: 10.1136/jmg.17.6.430
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318