Spondyloepiphyseal dysplasia (SED) is a descriptive term used for group of inherited disorders of bone growth resulting in short stature, skeletal abnormalities, and problems with hearing and vision. SED have three major forms, SED congenital, pseudoachondroplastic SED, and SED tarda. SED tarda is milder than SED congenita. True generalized microdontia is a rare condition in which all the teeth are abnormally small. This is a report of a rare case having SED with generalized microdontia in a 26-year-old patient
Type 2 collagen disorders encompass a diverse group of skeletal dysplasias that are commonly associa...
Ectodermal dysplasia is a rare hereditary disorder characterized by abnormal development of certain ...
International audienceBACKGROUND: Schimke immuno-osseous dysplasia (SIOD) is a rare, severe, autosom...
Copyright © 2013 Anita Singhal et al. This is an open access article distributed under the Creative ...
We report a case of sponastrime dysplasia (SEMDSP), which was diagnosed by characteristic clinical a...
Spondyloepiphysial dysplasia (SED) is a rare diseases which causes delayed growth, short statue and ...
Background: Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech (SED-BDS) is a syndrom...
Type 2 collagen disorders encompass a diverse group of skeletal dysplasias that are commonly associa...
Type 2 collagen disorders encompass a diverse group of skeletal dysplasias that are commonly associa...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
Recently a distinct spondyloepimetaphyseal dysplasia (SEMD) was reported in three members of a Jewis...
The authors describe the case of an Italian male aged 19 years who came to their observation for sev...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
Ectodermal dysplasia is a rare disease which affects at least two ectoderm-derived structures such a...
Cleidocranial Dysplasia(CCD) is an autosomal dominant human bone disease characterized by abnormal c...
Type 2 collagen disorders encompass a diverse group of skeletal dysplasias that are commonly associa...
Ectodermal dysplasia is a rare hereditary disorder characterized by abnormal development of certain ...
International audienceBACKGROUND: Schimke immuno-osseous dysplasia (SIOD) is a rare, severe, autosom...
Copyright © 2013 Anita Singhal et al. This is an open access article distributed under the Creative ...
We report a case of sponastrime dysplasia (SEMDSP), which was diagnosed by characteristic clinical a...
Spondyloepiphysial dysplasia (SED) is a rare diseases which causes delayed growth, short statue and ...
Background: Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech (SED-BDS) is a syndrom...
Type 2 collagen disorders encompass a diverse group of skeletal dysplasias that are commonly associa...
Type 2 collagen disorders encompass a diverse group of skeletal dysplasias that are commonly associa...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
Recently a distinct spondyloepimetaphyseal dysplasia (SEMD) was reported in three members of a Jewis...
The authors describe the case of an Italian male aged 19 years who came to their observation for sev...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
Ectodermal dysplasia is a rare disease which affects at least two ectoderm-derived structures such a...
Cleidocranial Dysplasia(CCD) is an autosomal dominant human bone disease characterized by abnormal c...
Type 2 collagen disorders encompass a diverse group of skeletal dysplasias that are commonly associa...
Ectodermal dysplasia is a rare hereditary disorder characterized by abnormal development of certain ...
International audienceBACKGROUND: Schimke immuno-osseous dysplasia (SIOD) is a rare, severe, autosom...