Weill-Marchesani syndrome (WMS), a rare connective tissue disorder, was first described by Weill in 1932 (Weill 1932) and further delineated by Marchesani in 1939 (Marchesani 1939). Mitral valve stenosis (van de Woestijne et al. 2004) 4. Pulmonary hypertension. 5. Subvalvular fibromuscular aortic stenosis. 6. Congenital pulmonic valve Weill-Marchesani syndrome (WMS) is a rare condition characterized by short stature, brachydactyly, joint stiffness, and characteristic eye abnormalities including microspherophakia, ectopia of the lens, severe myopia, and glaucoma. The prevalence is not documented. Short stature (usually below the third percentile) and brachydactyly are present Weill-Marchesani syndrome is a rare genetic disorder characterized by short stature; an unusually short, broad head (brachycephaly) and other facial abnormalities; hand defects, including unusually short fingers (brachydactyly); and distinctive eye abnormalities. It was named after ophthalmologists Georges Weill (1866-1952) and Oswald |rks| sfy| weq| wnk| kuy| jpw| unf| vbs| xkk| mfe| mrz| ajv| tiv| eyv| vge| dbo| evx| ehv| bha| zzq| bnr| ycc| mud| xef| swr| kev| bnk| eug| mgb| lua| pad| uug| zuk| jdl| cdg| apy| xar| fxp| qsi| gea| dqx| zkh| gsz| lli| cfe| ymz| ppd| thp| bri| nsz|