There are many different causes for corneal clouding/opacification which include both local ophthalmic causes as well as systemic causes. Mucopolysaccharidosis is a rare cause. Hence, we present a case of mucopolysaccharidosis type IV, who presented with bilateral corneal clouding and other systemic features of this storage disorder
Purpose. Maroteaux-Lamy syndrome is one of the mucopolysaccharidoses caused by enzyme deficiency (ar...
Corneal clouding or opacification is a prominent feature of mucopolysaccharidosis (MPS), particularl...
Mucous membrane pemphigoid (MMP) with ocular involvement, also referred to as ocular cicatricial pem...
Abstract: P>Ocular manifestations are very common in all types of mucopolysaccharidoses (MPS) and of...
A 44-year-old female patient presented to our department with bilateral corneal opacity since childh...
International audienceOcular pathology is common in patients with mucopolysaccharidosis (MPS), an he...
PURPOSE: Mucopolysaccharidoses (MPSs) are a rare group of lysosomal storage disorders characterized ...
Abstract Mucopolysaccharidoses (MPS) are a group of rare lysosomal storage disorders characterized b...
Ocular pathology is common in patients with mucopolysaccharidosis (MPS), a hereditary lysosomal stor...
Mucopolysaccharidoses (MPS) are a rare group of lysosomal storage disorders characterized by the acc...
Carlton R Fenzl,1 Kyla Teramoto,2 Majid Moshirfar3 1John A Moran Eye Center, University of Utah, Sa...
Abstract Mucopolysaccharidoses are a group of lysosomal storage disorders that are caused by deficie...
The purpose of this clinical case report is to describe a case of mucopolysaccharidosis type IVA (MP...
Corneal dystrophy is kind Groenouw an autosomal recessive disease whose gene is located in 16q22. It...
International audiencein Mucolipidosis Type IV A 7-year-old girl referred for a progressive bilatera...
Purpose. Maroteaux-Lamy syndrome is one of the mucopolysaccharidoses caused by enzyme deficiency (ar...
Corneal clouding or opacification is a prominent feature of mucopolysaccharidosis (MPS), particularl...
Mucous membrane pemphigoid (MMP) with ocular involvement, also referred to as ocular cicatricial pem...
Abstract: P>Ocular manifestations are very common in all types of mucopolysaccharidoses (MPS) and of...
A 44-year-old female patient presented to our department with bilateral corneal opacity since childh...
International audienceOcular pathology is common in patients with mucopolysaccharidosis (MPS), an he...
PURPOSE: Mucopolysaccharidoses (MPSs) are a rare group of lysosomal storage disorders characterized ...
Abstract Mucopolysaccharidoses (MPS) are a group of rare lysosomal storage disorders characterized b...
Ocular pathology is common in patients with mucopolysaccharidosis (MPS), a hereditary lysosomal stor...
Mucopolysaccharidoses (MPS) are a rare group of lysosomal storage disorders characterized by the acc...
Carlton R Fenzl,1 Kyla Teramoto,2 Majid Moshirfar3 1John A Moran Eye Center, University of Utah, Sa...
Abstract Mucopolysaccharidoses are a group of lysosomal storage disorders that are caused by deficie...
The purpose of this clinical case report is to describe a case of mucopolysaccharidosis type IVA (MP...
Corneal dystrophy is kind Groenouw an autosomal recessive disease whose gene is located in 16q22. It...
International audiencein Mucolipidosis Type IV A 7-year-old girl referred for a progressive bilatera...
Purpose. Maroteaux-Lamy syndrome is one of the mucopolysaccharidoses caused by enzyme deficiency (ar...
Corneal clouding or opacification is a prominent feature of mucopolysaccharidosis (MPS), particularl...
Mucous membrane pemphigoid (MMP) with ocular involvement, also referred to as ocular cicatricial pem...