This study reports a single case of Weill-Marchesani syndrome in an adult Nigerian. This syndrome is typically characterized by progressive joint stiffness, short stature, brachydactyly, microsherophakia and ectopia lentis. The patient had progressive loss of vision from bilateral cataract. To the best of our knowledge, there is no previously reported case of the syndrome in Africa. Key Words: Weill-Marchesani syndrome, Nigerian, cataract Nigerian Journal of Ophthalmology Vol.12 (1) 2004: 23-2
Anton–Babinski syndrome (Anton's syndrome) is well described in the scientific literature even thoug...
Purpose: To present a case of Weill-Marchesani syndrome with corneal endothelial dysfunction due to ...
Purpose: To describe clinical features in a large series of Möbius Syndrome (MBS) cases, investigati...
Weill Marchesani syndrome is a rare genetic disorder characterized by short stature, brachydactyly, ...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Background Weill-Marchesani syndrome is a rare systemic connective tissue disorder consisting of bra...
Weill–Marchesani syndrome is a rare connective tissue disorder, with a poorly understood etiology th...
THIS syndrome was first described by Marchesani (1939), and no case has hitherto been reported from ...
Morgagni hernia constitutes only about 2% of all diaphragmatic hernias and bilateral Morgagni hernia...
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who ...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
A case of Posner-Schlossman syndrome in an adult Nigerian male is reported. The patient presented at...
Aim: Waardenburg syndrome is a very rare condition, inherited autosomally with genetic heterogeneity...
Purpose: This study was designed to report the long-term complications of iris-claw phakic intraocul...
The Vogt-Koyanagl-Harada Syndrome is characterized by bilateral panuveitis and exudative retinal det...
Anton–Babinski syndrome (Anton's syndrome) is well described in the scientific literature even thoug...
Purpose: To present a case of Weill-Marchesani syndrome with corneal endothelial dysfunction due to ...
Purpose: To describe clinical features in a large series of Möbius Syndrome (MBS) cases, investigati...
Weill Marchesani syndrome is a rare genetic disorder characterized by short stature, brachydactyly, ...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Background Weill-Marchesani syndrome is a rare systemic connective tissue disorder consisting of bra...
Weill–Marchesani syndrome is a rare connective tissue disorder, with a poorly understood etiology th...
THIS syndrome was first described by Marchesani (1939), and no case has hitherto been reported from ...
Morgagni hernia constitutes only about 2% of all diaphragmatic hernias and bilateral Morgagni hernia...
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who ...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
A case of Posner-Schlossman syndrome in an adult Nigerian male is reported. The patient presented at...
Aim: Waardenburg syndrome is a very rare condition, inherited autosomally with genetic heterogeneity...
Purpose: This study was designed to report the long-term complications of iris-claw phakic intraocul...
The Vogt-Koyanagl-Harada Syndrome is characterized by bilateral panuveitis and exudative retinal det...
Anton–Babinski syndrome (Anton's syndrome) is well described in the scientific literature even thoug...
Purpose: To present a case of Weill-Marchesani syndrome with corneal endothelial dysfunction due to ...
Purpose: To describe clinical features in a large series of Möbius Syndrome (MBS) cases, investigati...