Twenty-nail dystrophy (TND) is an autosomal dominantly inherited idiopathic nail dystrophy characterized by excessive longitudinal striations and numerous superficial pits on nails with a typical 'sand papered' rough appearance. It is evident at birth and progresses slowly. It can also be associated with various diseases including lichen planus, alopecia areata, eczema, vitiligo and psoriasis. Peripheral blood chromosome analysis has not been performed in previously reported cases of TND. We report a mother and her 7-year-old daughter with TND. Both of them had a balanced translocation 46, XX, t(6q13;10p13). This may be a coincidental finding or may be related to the gene locus of TND
Human hereditary leukonychia is a rare nail disorder characterized by nail plates whitening on all f...
We describe 27 subjects (11 women) from five generations of a family with an apparently hitherto und...
<div><p>Pure hair and nail ectodermal dysplasia (PHNED) comprises a heterogeneous group of rare heri...
Isolated congenital nail dysplasia is an autosomal dominant disorder recently observed in a large fa...
Two siblings suffering from the so-called twenty-nail dystrophy are described. This syndrome is char...
We report on two sisters affected by congenital alopecia, nail dystrophy, and a severe T-cell immuno...
In dystrophic epidermolysis bullosa, the genetic defect of anchoring fibrils leads to cleavage benea...
Hereditary leukonychia (porcelain nails or white nails) is a rare nail disorder with an unknown gene...
Congenital Nail abnormalities are rare ectodermal defects. Autosomal recessive nail dysplasia is muc...
Isolated anonychia without any associated phenotypical disturbances is one of the rarest anomalies o...
Ectodermal dysplasia (ED) represents a heterogeneous group of genetic disorders characterized by the...
SummaryAutosomal dominant brachydactyly type B (BDB) is characterized by nail aplasia with rudimenta...
Hair and nail development have many similarities and are likely to share many developmental pathways...
Ectodermal dysplasia (ED) represents a heterogeneous group of genetic disorders characterized by the...
The nail patella syndrome (NPS1) is an autosomal dominant disorder characterised by dysplasia of the...
Human hereditary leukonychia is a rare nail disorder characterized by nail plates whitening on all f...
We describe 27 subjects (11 women) from five generations of a family with an apparently hitherto und...
<div><p>Pure hair and nail ectodermal dysplasia (PHNED) comprises a heterogeneous group of rare heri...
Isolated congenital nail dysplasia is an autosomal dominant disorder recently observed in a large fa...
Two siblings suffering from the so-called twenty-nail dystrophy are described. This syndrome is char...
We report on two sisters affected by congenital alopecia, nail dystrophy, and a severe T-cell immuno...
In dystrophic epidermolysis bullosa, the genetic defect of anchoring fibrils leads to cleavage benea...
Hereditary leukonychia (porcelain nails or white nails) is a rare nail disorder with an unknown gene...
Congenital Nail abnormalities are rare ectodermal defects. Autosomal recessive nail dysplasia is muc...
Isolated anonychia without any associated phenotypical disturbances is one of the rarest anomalies o...
Ectodermal dysplasia (ED) represents a heterogeneous group of genetic disorders characterized by the...
SummaryAutosomal dominant brachydactyly type B (BDB) is characterized by nail aplasia with rudimenta...
Hair and nail development have many similarities and are likely to share many developmental pathways...
Ectodermal dysplasia (ED) represents a heterogeneous group of genetic disorders characterized by the...
The nail patella syndrome (NPS1) is an autosomal dominant disorder characterised by dysplasia of the...
Human hereditary leukonychia is a rare nail disorder characterized by nail plates whitening on all f...
We describe 27 subjects (11 women) from five generations of a family with an apparently hitherto und...
<div><p>Pure hair and nail ectodermal dysplasia (PHNED) comprises a heterogeneous group of rare heri...