Rhizomelic chondrodysplasia punctate (RCDP) is a rare autosomal recessive peroxisomal disease. The main features of the disease are shortening of the proximal long bones, punctate calcifications located in the epiphyses of long bones and in soft tissues around joints and vertebral column, vertebral clefting, dysmorphic face, and severe growth retardation, whereas cervical spinal stenosis may also rarely be present. Imaging of the brain and spinal cord in patients with this disorder may aid prognosis and guide management decisions. We report the newborn diagnosed as CDP with cervical stenosis. Our aim is to discuss current knowledge on etiopathogenesis as well as radiological and clinical symptoms of diseases associated w...
Hadeel Alrukban,1 David Chitayat1,2 1Department of Pediatrics, Division of Clinical and Metabolic Ge...
Background Rhizomelic chondrodysplasia punctata (RCDP) type 1 is among of the rare autosomal recessi...
Chondrodysplasia punctata (CDP) is associated with a variety of genetic and nongenetic conditions. W...
Copyright © 2014 Nalan Karabayır et al.This is an open access article distributed under theCreativeC...
Background: Chondrodysplasia punctata (CDP) is a rare, heterogeneous congenital skeletal dysplasia, ...
We are reporting a 3-month-old male child who presented to us with growth failure, but detailed eval...
BACKGROUND & OBJECTIVE: Chondrodysplasia punctata (CPD) describes a diverse group of bony dysplasias...
Key Clinical Message Rhizomelic chondrodysplasia punctata (RCDP) is a rare disorder (~1 in 100,000 l...
Rhizomelic chondrodysplasia punctata (RCDP) is a heterogenous group of disorders due to defects in g...
Brachytelephalangic chondrodysplasia punctata (CDPX1, OMIM: #302950) is a rare congenital skeletal d...
To describe the neurologic profiles of Rhizomelic chondrodysplasia punctata (RCDP); a peroxisomal di...
Abstract Background Rhizomelic chondrodysplasia punctata (RCDP) is a clinical entity resulting from ...
Rhizomelic chondrodysplasia punctata type 1 is an inherited disease with extremely rare presentation...
International audienceWe report the prenatal management of a brachytelephalangic chondrodysplasia pu...
Chondrodysplasia calcificans punctata (CDP) is a rare congenital syndrome characterized by calcific ...
Hadeel Alrukban,1 David Chitayat1,2 1Department of Pediatrics, Division of Clinical and Metabolic Ge...
Background Rhizomelic chondrodysplasia punctata (RCDP) type 1 is among of the rare autosomal recessi...
Chondrodysplasia punctata (CDP) is associated with a variety of genetic and nongenetic conditions. W...
Copyright © 2014 Nalan Karabayır et al.This is an open access article distributed under theCreativeC...
Background: Chondrodysplasia punctata (CDP) is a rare, heterogeneous congenital skeletal dysplasia, ...
We are reporting a 3-month-old male child who presented to us with growth failure, but detailed eval...
BACKGROUND & OBJECTIVE: Chondrodysplasia punctata (CPD) describes a diverse group of bony dysplasias...
Key Clinical Message Rhizomelic chondrodysplasia punctata (RCDP) is a rare disorder (~1 in 100,000 l...
Rhizomelic chondrodysplasia punctata (RCDP) is a heterogenous group of disorders due to defects in g...
Brachytelephalangic chondrodysplasia punctata (CDPX1, OMIM: #302950) is a rare congenital skeletal d...
To describe the neurologic profiles of Rhizomelic chondrodysplasia punctata (RCDP); a peroxisomal di...
Abstract Background Rhizomelic chondrodysplasia punctata (RCDP) is a clinical entity resulting from ...
Rhizomelic chondrodysplasia punctata type 1 is an inherited disease with extremely rare presentation...
International audienceWe report the prenatal management of a brachytelephalangic chondrodysplasia pu...
Chondrodysplasia calcificans punctata (CDP) is a rare congenital syndrome characterized by calcific ...
Hadeel Alrukban,1 David Chitayat1,2 1Department of Pediatrics, Division of Clinical and Metabolic Ge...
Background Rhizomelic chondrodysplasia punctata (RCDP) type 1 is among of the rare autosomal recessi...
Chondrodysplasia punctata (CDP) is associated with a variety of genetic and nongenetic conditions. W...