Geleophysic dysplasia and Weill-Marchesani syndrome are acromelic dysplasias characterized by short stature, brachydactyly, and joint contractures. Recessive Weill-Marchesani syndrome typically includes spherophakia, but the ocular phenotype of recessive geleophysic dysplasia is not well defined. We describe the ocular phenotype of a girl with genetically confirmed recessive geleophysic dysplasia (biallelic ADAMTSL2 mutations). Features included high corneal astigmatism, accommodative esotropia, unilateral Brown syndrome, and no evidence for zonular disease at 12 years of age
Geleophysic dysplasia (GPHYSD1, MIM231050; GPHYSD2, MIM614185; GPHYSD3, MIM617809) is an autosomal d...
Image shows a patient with the Laurence-Moon-Biedl syndrome, an autosomal recessive syndrome charact...
Background Knobloch syndrome is defined as a triad of occipital defect, high myopia and vitreo-retin...
Geleophysic dysplasia and Weill-Marchesani syndrome are acromelic dysplasias characterized by short ...
The acromelic dysplasias comprise short stature, hands and feet, and stiff joints. Three disorders a...
Background: Geleophysic dysplasia and Weill-Marchesani syndrome from the acromelic dysplasias group ...
The acromelic dysplasias comprise short stature, hands and feet, and stiff joints. Three disorders a...
Background. Geleophysic dysplasia is a rare multisystem disorder that principally affects the bones,...
Weill Marchesani syndrome is a rare genetic disorder characterized by short stature, brachydactyly, ...
Geleophysic dysplasia (GD, OMIM 231050) is an autosomal recessive disorder characterised by short st...
Background Geleophysic dysplasia (GD, OMIM 231050) is an autosomal recessive disorder characterised ...
Brown syndrome is a rare mechanical disorder characterized by restriction of the superior oblique tr...
International audienceGeleophysic dysplasia (OMIM 231050, GD) is an autosomal recessive disorder cha...
Background Weill-Marchesani syndrome is a rare systemic connective tissue disorder consisting of bra...
BackgroundGeleophysic dysplasia is an extremely rare autosomal recessive acromelic skeletal dysplasi...
Geleophysic dysplasia (GPHYSD1, MIM231050; GPHYSD2, MIM614185; GPHYSD3, MIM617809) is an autosomal d...
Image shows a patient with the Laurence-Moon-Biedl syndrome, an autosomal recessive syndrome charact...
Background Knobloch syndrome is defined as a triad of occipital defect, high myopia and vitreo-retin...
Geleophysic dysplasia and Weill-Marchesani syndrome are acromelic dysplasias characterized by short ...
The acromelic dysplasias comprise short stature, hands and feet, and stiff joints. Three disorders a...
Background: Geleophysic dysplasia and Weill-Marchesani syndrome from the acromelic dysplasias group ...
The acromelic dysplasias comprise short stature, hands and feet, and stiff joints. Three disorders a...
Background. Geleophysic dysplasia is a rare multisystem disorder that principally affects the bones,...
Weill Marchesani syndrome is a rare genetic disorder characterized by short stature, brachydactyly, ...
Geleophysic dysplasia (GD, OMIM 231050) is an autosomal recessive disorder characterised by short st...
Background Geleophysic dysplasia (GD, OMIM 231050) is an autosomal recessive disorder characterised ...
Brown syndrome is a rare mechanical disorder characterized by restriction of the superior oblique tr...
International audienceGeleophysic dysplasia (OMIM 231050, GD) is an autosomal recessive disorder cha...
Background Weill-Marchesani syndrome is a rare systemic connective tissue disorder consisting of bra...
BackgroundGeleophysic dysplasia is an extremely rare autosomal recessive acromelic skeletal dysplasi...
Geleophysic dysplasia (GPHYSD1, MIM231050; GPHYSD2, MIM614185; GPHYSD3, MIM617809) is an autosomal d...
Image shows a patient with the Laurence-Moon-Biedl syndrome, an autosomal recessive syndrome charact...
Background Knobloch syndrome is defined as a triad of occipital defect, high myopia and vitreo-retin...