El síndrome de Weill-Marchesani es un desorden genético poco frecuente del tejido conectivo con afectación ocular. Desde su descripción por Weill y Marchesani en 1932 y 1939, se han descrito patrones de herencia autosómica dominante y recesiva. En general estos pacientes se caracterizan por baja talla, braquidactilia con rigidez articular, microsferofaquia, miopía lenticular progresiva, luxación cristaliniana, y glaucoma secundario. Se presentan las características oftalmológicas y clínicas de una paciente a quien se le diagnosticó este síndrome genético. Procedía de una familia de 4 miembros donde uno de ellos presentaba similares características (padre), no se detectaron malformaciones cardiovasculares asociadas pero se recogen antecedent...
Weill Marchesani Syndrome (WMS) is an unusual systemic connective tissue disorder. This case report ...
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who ...
Geleophysic dysplasia and Weill-Marchesani syndrome are acromelic dysplasias characterized by short ...
Weill Marchesani syndrome is a rare genetic disorder characterized by short stature, brachydactyly, ...
Background Weill-Marchesani syndrome is a rare systemic connective tissue disorder consisting of bra...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Weill–Marchesani syndrome is a rare connective tissue disorder, with a poorly understood etiology th...
This study reports a single case of Weill-Marchesani syndrome in an adult Nigerian. This syndrome is...
Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterised by short stature, brac...
Desde 1880 Von Graefe y Saemish agruparon algunos pacientes con trastornos congénitos infrecuentes d...
Marfan’s syndrome is an autosomal dominant inheritance disorder that affects many body systems (skel...
Objetivo: Para se identificar as alterações oculares presentes na síndrome de Marfan, este trabalho ...
In 1880 Von Graefe and Saemish grouped some patients with infrequent non progressive congenital di...
Se presentan las características oftalmológicas y clínicas de dos pacientes hermanos (hembra y varón...
The acromelic dysplasias comprise short stature, hands and feet, and stiff joints. Three disorders a...
Weill Marchesani Syndrome (WMS) is an unusual systemic connective tissue disorder. This case report ...
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who ...
Geleophysic dysplasia and Weill-Marchesani syndrome are acromelic dysplasias characterized by short ...
Weill Marchesani syndrome is a rare genetic disorder characterized by short stature, brachydactyly, ...
Background Weill-Marchesani syndrome is a rare systemic connective tissue disorder consisting of bra...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Weill–Marchesani syndrome is a rare connective tissue disorder, with a poorly understood etiology th...
This study reports a single case of Weill-Marchesani syndrome in an adult Nigerian. This syndrome is...
Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterised by short stature, brac...
Desde 1880 Von Graefe y Saemish agruparon algunos pacientes con trastornos congénitos infrecuentes d...
Marfan’s syndrome is an autosomal dominant inheritance disorder that affects many body systems (skel...
Objetivo: Para se identificar as alterações oculares presentes na síndrome de Marfan, este trabalho ...
In 1880 Von Graefe and Saemish grouped some patients with infrequent non progressive congenital di...
Se presentan las características oftalmológicas y clínicas de dos pacientes hermanos (hembra y varón...
The acromelic dysplasias comprise short stature, hands and feet, and stiff joints. Three disorders a...
Weill Marchesani Syndrome (WMS) is an unusual systemic connective tissue disorder. This case report ...
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who ...
Geleophysic dysplasia and Weill-Marchesani syndrome are acromelic dysplasias characterized by short ...