Add to ORKGChanarin-Dorfman syndrome (CDS) is a very rare autosomal recessive inherited neutral lipid metabolism disorder associated with congenital ichthyosis and multi-system involvement. Observation of lipid vacuoles in neutrophils (Jordan’s anomaly) in peripheral blood smears in patients with ichthyosiform erythroderma is diagnostic. Herein we present
Chanarin-Dorfman Syndrome (CDS) is caused by a defect in the CGI-58/ABHD5 gene resulting in a defici...
Chanarin-Dorfman Syndrome (CDS) is caused by a defect in the CGI-58/ABHD5 gene resulting in a defici...
PubMedID: 17095855Background: Dorfman-Chanarin syndrome is a rare, autosomal recessive, inherited, l...
Chanarin-Dorfman syndrome (CDS) is a very rare autosomal recessive inherited neutral lipid metabolis...
Chanarin-Dorfman syndrome (CDS) is a very rare autosomal recessive inherited neutral lipid metabolis...
Chanarin-Dorfman syndrome (CDS) is a rare, autosomal recessive inherited lipid storage disease with ...
Chanarin Dorfman syndrome (CDS) is a very rare neutral lipid metabolism disorder with multisystem in...
Chanarin Dorfman Syndrome is a multisystem inherited metabolic disorder associated with congenital i...
Abstract Background Chanarin Dorfman Syndrome (CDS) is a rare autosomal recessive disorder character...
We describe the clinical features, muscle pathology features, and molecular studies of seven patient...
We describe the clinical features, muscle pathology features, and molecular studies of seven patient...
Dorfman-Chanarin syndrome is a rare autosomal recessive neutral lipid storage disorder with congenit...
Dorfman-Chanarin syndrome is a rare, autosomal recessive disorder characterized by congenital ichthy...
Chanarin Dorfman syndrome is a multisystem, very rare, autosomal recessive lipid storage disorder, c...
Chanarin-Dorfman Syndrome (CDS) is caused by a defect in the CGI-58/ABHD5 gene resulting in a defici...
Chanarin-Dorfman Syndrome (CDS) is caused by a defect in the CGI-58/ABHD5 gene resulting in a defici...
PubMedID: 17095855Background: Dorfman-Chanarin syndrome is a rare, autosomal recessive, inherited, l...
Chanarin-Dorfman syndrome (CDS) is a very rare autosomal recessive inherited neutral lipid metabolis...
Chanarin-Dorfman syndrome (CDS) is a very rare autosomal recessive inherited neutral lipid metabolis...
Chanarin-Dorfman syndrome (CDS) is a rare, autosomal recessive inherited lipid storage disease with ...
Chanarin Dorfman syndrome (CDS) is a very rare neutral lipid metabolism disorder with multisystem in...
Chanarin Dorfman Syndrome is a multisystem inherited metabolic disorder associated with congenital i...
Abstract Background Chanarin Dorfman Syndrome (CDS) is a rare autosomal recessive disorder character...
We describe the clinical features, muscle pathology features, and molecular studies of seven patient...
We describe the clinical features, muscle pathology features, and molecular studies of seven patient...
Dorfman-Chanarin syndrome is a rare autosomal recessive neutral lipid storage disorder with congenit...
Dorfman-Chanarin syndrome is a rare, autosomal recessive disorder characterized by congenital ichthy...
Chanarin Dorfman syndrome is a multisystem, very rare, autosomal recessive lipid storage disorder, c...
Chanarin-Dorfman Syndrome (CDS) is caused by a defect in the CGI-58/ABHD5 gene resulting in a defici...
Chanarin-Dorfman Syndrome (CDS) is caused by a defect in the CGI-58/ABHD5 gene resulting in a defici...
PubMedID: 17095855Background: Dorfman-Chanarin syndrome is a rare, autosomal recessive, inherited, l...