Purpose Cartilage hair hypoplasia (CHH) is a rare metaphyseal chondrodysplasia characterized by short sta-ture and short limbs, found primarily in Amish and Finnish populations. Cartilage hair hypoplasia is caused by muta-tions in the RMRP gene located on chromosome 9p13.3. The disorder has several characteristic orthopaedic manifestations, including joint laxity, limited elbow ex-tension, ankle varus, and genu varum. Immunodeficiency is of concern in most cases. Although patients exhibit orthopaedic problems, the orthopaedic literature on CHH patients is scant at best. The objective of this study was to characterize the orthopaedic manifestations of CHH based on the authors ’ unique access to the largest collection of CHH patients ever rep...
Cartilage-hair hypoplasia (CHH) is a rare autosomal recessive disease caused by mutations in the RMR...
The chondrodysplasias are a group of genetic disorders resulting from profound defects in cartilage ...
BackgroundCartilage-hair hypoplasia (MIM 250250) is an autosomal recessive disease with diverse clin...
Context: Cartilage-hair hypoplasia is a rare hereditary cause of short stature. The aim of this stud...
Review on Cartilage-hair hypoplasia (CHH), with data on clinics, and the genes involved
Six cases of cartilage hair hypoplasia from five kindreds are described. They demonstrate variation ...
We describe 7 cases of cartilage hair hypoplasia (CHH) with emphasis on the clinical and immunologic...
A porc-haj hypoplasia ritka, autoszomális recesszív öröklődésmenetű primer immunhiány-betegség, amel...
Contains fulltext : 22098___.PDF (publisher's version ) (Open Access
BackgroundBiallelic mutations in the non-coding RNA gene RMRP cause Cartilage-hair hypoplasia (CHH),...
Introduction: Brief overview of Bone Development Disorders of the Skeleton Cartilage-Hair-Hypoplasia...
Mutations in the RMRP gene that codes for an RNA subunit of the MRP RNAse complex are the cause of c...
Mutations in the RMRP gene that codes for an RNA subunit of the MRP RNAse complex are the cause of c...
Background: Cartilage-hair hypoplasia (CHH) is a rare chondrodysplasia, including disproportionate s...
Cartilage-hair hypoplasia syndrome (CHH) is an autosomal recessive disorder caused by pathogenic var...
Cartilage-hair hypoplasia (CHH) is a rare autosomal recessive disease caused by mutations in the RMR...
The chondrodysplasias are a group of genetic disorders resulting from profound defects in cartilage ...
BackgroundCartilage-hair hypoplasia (MIM 250250) is an autosomal recessive disease with diverse clin...
Context: Cartilage-hair hypoplasia is a rare hereditary cause of short stature. The aim of this stud...
Review on Cartilage-hair hypoplasia (CHH), with data on clinics, and the genes involved
Six cases of cartilage hair hypoplasia from five kindreds are described. They demonstrate variation ...
We describe 7 cases of cartilage hair hypoplasia (CHH) with emphasis on the clinical and immunologic...
A porc-haj hypoplasia ritka, autoszomális recesszív öröklődésmenetű primer immunhiány-betegség, amel...
Contains fulltext : 22098___.PDF (publisher's version ) (Open Access
BackgroundBiallelic mutations in the non-coding RNA gene RMRP cause Cartilage-hair hypoplasia (CHH),...
Introduction: Brief overview of Bone Development Disorders of the Skeleton Cartilage-Hair-Hypoplasia...
Mutations in the RMRP gene that codes for an RNA subunit of the MRP RNAse complex are the cause of c...
Mutations in the RMRP gene that codes for an RNA subunit of the MRP RNAse complex are the cause of c...
Background: Cartilage-hair hypoplasia (CHH) is a rare chondrodysplasia, including disproportionate s...
Cartilage-hair hypoplasia syndrome (CHH) is an autosomal recessive disorder caused by pathogenic var...
Cartilage-hair hypoplasia (CHH) is a rare autosomal recessive disease caused by mutations in the RMR...
The chondrodysplasias are a group of genetic disorders resulting from profound defects in cartilage ...
BackgroundCartilage-hair hypoplasia (MIM 250250) is an autosomal recessive disease with diverse clin...