Dermatopathia pigmentosa reticularis and overlap syndrome in siblings-A rare case report. [PDF]
Raj M +6 more
europepmc +1 more source
Integrated Prosthodontic Approach for Ectodermal Dysplasia: Tooth-Supported Overdenture and Implant-Supported Hybrid Prosthesis. [PDF]
Saini A +4 more
europepmc +1 more source
Disease-associated NEMO mutations as a tool to unravel the key molecular mechanisms in NF-kappaB activation [PDF]
Pescatore, Alessandra
core
Syndromic and Non-Syndromic Primary Failure of Tooth Eruption: A Genetic Overview. [PDF]
Modafferi C +3 more
europepmc +1 more source
Genodermatosis among the southwestern Saudi population: The pattern and the need for a premarital genetic screening protocol. [PDF]
Alfahaad HA.
europepmc +1 more source
Prenatal sonographic evidence of hypohidrotic ectodermal dysplasia and postnatal genetic testing of a family line of child. [PDF]
Lin D +9 more
europepmc +1 more source
Prenatal genetic testing and potential consequences. [PDF]
Jauch SF, Klaritsch P.
europepmc +1 more source
A missense mutation in the highly conserved TNF-like domain of Ectodysplasin A is the candidate causative variant for X-linked hypohidrotic ectodermal dysplasia in Limousin cattle: Clinical, histological, and molecular analyses. [PDF]
Krull F, Bleyer M, Schäfer J, Brenig B.
europepmc +1 more source
Nasopharyngeal rhabdomyosarcoma in a patient with hypohidrotic ectodermal dysplasia syndrome
Hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome) is characterized by partial or complete absence of sweat glands, hypotrichosis, hypodontia, prominent frontal ridges and chin, saddle nose, sunken cheeks, thick, everted lips, large ...
Ahmet Metin +2 more
exaly +2 more sources

