Add to ORKGThe Witkop syndrome, also known as the “tooth and nail syndrome” (TNS) or “nail dysgenesis and hypodontia”, is a form of ectodermal dysplasia, a group of hereditary diseases characterized by the absence or impaired function of two or more ectodermally derived structure
Other names Keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis. Eccrine tum...
Mutations in the TP63 gene have been associated with a variety of ectodermal dysplasia syndromes, am...
Ectodermal dysplasia-skin fragility syndrome is a rare autosomal recessive inherited disease charact...
Witkop′s tooth and nail syndrome is a rare autosomal dominant disorder of ectodermal dysplasi...
Witkop syndrome, also known as tooth and nail syndrome (TNS), is a rare autosomal dominant disorder....
Tooth and Nail Syndrome or Nail Dysplasias with Hypodontiaor Witkop´s Syndrome is an autosomal domin...
EDSS1, a syndrome characterized by ectodermal dysplasia-syndactyly, is inherited in an autosomal rec...
The Msx1 transcription factor is involved in multiple epithelial-mesenchymal interactions during ver...
The Msx1 transcription factor is involved in multiple epithelial-mesenchymal interactions during ver...
The ectodermal dysplasias (ED) are a large and complex group of diseases characterized by anomalies ...
The ectodermal dysplasias (ED) are a large and complex group of diseases characterized by anomalies ...
PurposeNail-Patella syndrome is a dominantly inherited genetic disorder characterized by abnormaliti...
Abstract Background Pure hair and nail ectodermal dysplasia (PHNED) is a congenital disorder of hair...
Desmosomal genodermatoses are a heterogeneous group of in-herited diseases caused by defective desmo...
MSX1 mutations have been reported in four unrelated families with autosomal dominant tooth agenesis....
Other names Keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis. Eccrine tum...
Mutations in the TP63 gene have been associated with a variety of ectodermal dysplasia syndromes, am...
Ectodermal dysplasia-skin fragility syndrome is a rare autosomal recessive inherited disease charact...
Witkop′s tooth and nail syndrome is a rare autosomal dominant disorder of ectodermal dysplasi...
Witkop syndrome, also known as tooth and nail syndrome (TNS), is a rare autosomal dominant disorder....
Tooth and Nail Syndrome or Nail Dysplasias with Hypodontiaor Witkop´s Syndrome is an autosomal domin...
EDSS1, a syndrome characterized by ectodermal dysplasia-syndactyly, is inherited in an autosomal rec...
The Msx1 transcription factor is involved in multiple epithelial-mesenchymal interactions during ver...
The Msx1 transcription factor is involved in multiple epithelial-mesenchymal interactions during ver...
The ectodermal dysplasias (ED) are a large and complex group of diseases characterized by anomalies ...
The ectodermal dysplasias (ED) are a large and complex group of diseases characterized by anomalies ...
PurposeNail-Patella syndrome is a dominantly inherited genetic disorder characterized by abnormaliti...
Abstract Background Pure hair and nail ectodermal dysplasia (PHNED) is a congenital disorder of hair...
Desmosomal genodermatoses are a heterogeneous group of in-herited diseases caused by defective desmo...
MSX1 mutations have been reported in four unrelated families with autosomal dominant tooth agenesis....
Other names Keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis. Eccrine tum...
Mutations in the TP63 gene have been associated with a variety of ectodermal dysplasia syndromes, am...
Ectodermal dysplasia-skin fragility syndrome is a rare autosomal recessive inherited disease charact...