Chondrodysplasia punctata (CDP) is associated with a variety of genetic and nongenetic conditions. We report a girl with CDP, complex congenital cardiac disease, central nervous system (CNS) anomalies, and clinical findings that resemble those of the sibs described by Toriello et al. [1993, Am J Med Genet 47:797-799]. The cardiac defects and CNS abnormalities reported are unique in the context of CDP and may serve to expand the phenotypic spectrum of the unique form of CDP described by Toriello et al. [1993].3 page(s
Brachytelephalangic chondrodysplasia punctata (CDPX1, OMIM: #302950) is a rare congenital skeletal d...
Rhizomelic chondrodysplasia punctate (RCDP) is a rare autosomal recessive peroxisomal disease. The m...
International audienceObjectivesConradi-Hunermann-Happle [X-linked dominant chondrodysplasia punctat...
Background: Chondrodysplasia punctata (CDP) is a rare, heterogeneous congenital skeletal dysplasia, ...
BACKGROUND & OBJECTIVE: Chondrodysplasia punctata (CPD) describes a diverse group of bony dysplasias...
Includes bibliographical references (pages 88-125)X-linked dominant Chondrodysplasia Punctata (CDPX2...
X-linked chondrodysplasia punctata 1 (CDPX1), a congenital disorder of bone and cartilage developmen...
The term, "chondrodysplasia punctata" (CDP) denotes a pattern of abnormal punctate calcification of ...
Copyright © 2014 Nalan Karabayır et al.This is an open access article distributed under theCreativeC...
Hadeel Alrukban,1 David Chitayat1,2 1Department of Pediatrics, Division of Clinical and Metabolic Ge...
International audienceWe report the prenatal management of a brachytelephalangic chondrodysplasia pu...
Chondrodysplasia calcificans punctata (CDP) is a rare congenital syndrome characterized by calcific ...
The chondrodysplasia punctatas (CDP) are a group of genetic diseases presenting with the common hall...
Brachytelephalangic chondrodysplasia punctata (CDPX1, OMIM: #302950) is a rare congenital skeletal d...
Rhizomelic chondrodysplasia punctate (RCDP) is a rare autosomal recessive peroxisomal disease. The m...
International audienceObjectivesConradi-Hunermann-Happle [X-linked dominant chondrodysplasia punctat...
Background: Chondrodysplasia punctata (CDP) is a rare, heterogeneous congenital skeletal dysplasia, ...
BACKGROUND & OBJECTIVE: Chondrodysplasia punctata (CPD) describes a diverse group of bony dysplasias...
Includes bibliographical references (pages 88-125)X-linked dominant Chondrodysplasia Punctata (CDPX2...
X-linked chondrodysplasia punctata 1 (CDPX1), a congenital disorder of bone and cartilage developmen...
The term, "chondrodysplasia punctata" (CDP) denotes a pattern of abnormal punctate calcification of ...
Copyright © 2014 Nalan Karabayır et al.This is an open access article distributed under theCreativeC...
Hadeel Alrukban,1 David Chitayat1,2 1Department of Pediatrics, Division of Clinical and Metabolic Ge...
International audienceWe report the prenatal management of a brachytelephalangic chondrodysplasia pu...
Chondrodysplasia calcificans punctata (CDP) is a rare congenital syndrome characterized by calcific ...
The chondrodysplasia punctatas (CDP) are a group of genetic diseases presenting with the common hall...
Brachytelephalangic chondrodysplasia punctata (CDPX1, OMIM: #302950) is a rare congenital skeletal d...
Rhizomelic chondrodysplasia punctate (RCDP) is a rare autosomal recessive peroxisomal disease. The m...
International audienceObjectivesConradi-Hunermann-Happle [X-linked dominant chondrodysplasia punctat...