A porc-haj hypoplasia ritka, autoszomális recesszív öröklődésmenetű primer immunhiány-betegség, amelyre a döntően T-sejtes immundeficiencia mellett metaphysealis chondrodysplasia jellemző. A közleményben a szerzők egy esetismertetés kapcsán mutatják be a betegség klinikumát és a jellemző laboratóriumi leleteket, összefoglalják a kórkép molekuláris patomechanizmusával kapcsolatos ismereteket és a kezelés lehetőségeit. | Cartilage-hair hypoplasia is a rare, autosomal recessive primary immunodeficiency disorder characterized by predominantly T-cell deficiency and metaphyseal chondrodysplasia. The authors summarize current knowledge on molecular genetics, diagnostic characteristics and therapeutic options of this inherited immunodefi...
Focal dermal hypoplasia (FDH), or Goltz syndrome, is a rare X-linked dominant ectodermal and mesoder...
Cartilage-hair hypoplasia and anauxetic dysplasia are two autosomal recessive skeletal dysplasias ch...
Contains fulltext : 81709.pdf (publisher's version ) (Closed access)The X-linked d...
Contains fulltext : 22098___.PDF (publisher's version ) (Open Access
Purpose Cartilage hair hypoplasia (CHH) is a rare metaphyseal chondrodysplasia characterized by shor...
Context: Cartilage-hair hypoplasia is a rare hereditary cause of short stature. The aim of this stud...
BackgroundCartilage-hair hypoplasia (MIM 250250) is an autosomal recessive disease with diverse clin...
Six cases of cartilage hair hypoplasia from five kindreds are described. They demonstrate variation ...
Cartilage hair hypoplasia syndrome (OMIM # 250250) is a rare autosomal recessive metaphyseal dysplas...
Review on Cartilage-hair hypoplasia (CHH), with data on clinics, and the genes involved
We describe 7 cases of cartilage hair hypoplasia (CHH) with emphasis on the clinical and immunologic...
Cartilage-hair hypoplasia (CHH) is an autosomal recessive syndromic immunodeficiency with skeletal d...
Cartilage-hair hypoplasia (CHH) is a rare autosomal recessive disease caused by mutations in the RMR...
Introduction: Brief overview of Bone Development Disorders of the Skeleton Cartilage-Hair-Hypoplasia...
Background: Cartilage-hair hypoplasia (CHH) is a rare chondrodysplasia, including disproportionate s...
Focal dermal hypoplasia (FDH), or Goltz syndrome, is a rare X-linked dominant ectodermal and mesoder...
Cartilage-hair hypoplasia and anauxetic dysplasia are two autosomal recessive skeletal dysplasias ch...
Contains fulltext : 81709.pdf (publisher's version ) (Closed access)The X-linked d...
Contains fulltext : 22098___.PDF (publisher's version ) (Open Access
Purpose Cartilage hair hypoplasia (CHH) is a rare metaphyseal chondrodysplasia characterized by shor...
Context: Cartilage-hair hypoplasia is a rare hereditary cause of short stature. The aim of this stud...
BackgroundCartilage-hair hypoplasia (MIM 250250) is an autosomal recessive disease with diverse clin...
Six cases of cartilage hair hypoplasia from five kindreds are described. They demonstrate variation ...
Cartilage hair hypoplasia syndrome (OMIM # 250250) is a rare autosomal recessive metaphyseal dysplas...
Review on Cartilage-hair hypoplasia (CHH), with data on clinics, and the genes involved
We describe 7 cases of cartilage hair hypoplasia (CHH) with emphasis on the clinical and immunologic...
Cartilage-hair hypoplasia (CHH) is an autosomal recessive syndromic immunodeficiency with skeletal d...
Cartilage-hair hypoplasia (CHH) is a rare autosomal recessive disease caused by mutations in the RMR...
Introduction: Brief overview of Bone Development Disorders of the Skeleton Cartilage-Hair-Hypoplasia...
Background: Cartilage-hair hypoplasia (CHH) is a rare chondrodysplasia, including disproportionate s...
Focal dermal hypoplasia (FDH), or Goltz syndrome, is a rare X-linked dominant ectodermal and mesoder...
Cartilage-hair hypoplasia and anauxetic dysplasia are two autosomal recessive skeletal dysplasias ch...
Contains fulltext : 81709.pdf (publisher's version ) (Closed access)The X-linked d...