Results 231 to 240 of about 128,250 (259)
Some of the next articles are maybe not open access.
Journal of Cutaneous Pathology, 2012
Localized longitudinal erythronychia describes a solitary red streak limited to a single nail unit. Localized longitudinal erythronychia can be caused by both benign and malignant entities. Most commonly, the cause is a benign process, such as an onychopapilloma.
Suthinee, Rutnin +4 more
openaire +2 more sources
Localized longitudinal erythronychia describes a solitary red streak limited to a single nail unit. Localized longitudinal erythronychia can be caused by both benign and malignant entities. Most commonly, the cause is a benign process, such as an onychopapilloma.
Suthinee, Rutnin +4 more
openaire +2 more sources
Hypohidrotic Ectodermal Dysplasia: A Rare Disorder With Bilateral Infantile Glaucoma
Journal of glaucoma, 2019Ectodermal dysplasia (ED) is a disorder that occurs due to abnormalities of ectodermal structures such as skin, teeth, hair, nails, and eccrine glands. Approximately 200 different conditions have been identified as ED, the most common being hypohidrotic ...
S. Dubey, M. Bhoot, Kanika Jain
semanticscholar +1 more source
Revue de Chirurgie Orthopédique et Traumatologique, 2013
Summary Nail-patella syndrome (NPS) or hereditary onycho-osteodysplasia is a relatively rare autosomal dominant disorder with the classic tetrad of fingernail abnormalities, hypoplastic patellae, radial head dislocation and iliac horns. The anatomic abnormalities in NPS often lead to subluxation or dislocation of the patellae causing knee instability
S. Lippacher +3 more
openaire +1 more source
Summary Nail-patella syndrome (NPS) or hereditary onycho-osteodysplasia is a relatively rare autosomal dominant disorder with the classic tetrad of fingernail abnormalities, hypoplastic patellae, radial head dislocation and iliac horns. The anatomic abnormalities in NPS often lead to subluxation or dislocation of the patellae causing knee instability
S. Lippacher +3 more
openaire +1 more source
American Journal of Medical Genetics Part A, 2012
AbstractThe Simpson–Golabi–Behmel syndrome type 1 (SGBS1, OMIM #312870) is an X‐linked overgrowth condition comprising abnormal facial appearance, supernumerary nipples, congenital heart defects, polydactyly, fingernail hypoplasia, increased risk of neonatal death and of neoplasia. It is caused by mutation/deletion of the GPC3 gene.
Garavelli, L. +14 more
openaire +3 more sources
AbstractThe Simpson–Golabi–Behmel syndrome type 1 (SGBS1, OMIM #312870) is an X‐linked overgrowth condition comprising abnormal facial appearance, supernumerary nipples, congenital heart defects, polydactyly, fingernail hypoplasia, increased risk of neonatal death and of neoplasia. It is caused by mutation/deletion of the GPC3 gene.
Garavelli, L. +14 more
openaire +3 more sources
King Khalid University Journal of Health Sciences
Ectodermal dysplasia is a rare hereditary disorder characterized by the abnormal development of ectodermal tissues. Hidrotic and hypohidrotic ectodermal dysplasia are the two most common types of the disease. The typical oral features include malformed
L. Aldosari
semanticscholar +1 more source
Ectodermal dysplasia is a rare hereditary disorder characterized by the abnormal development of ectodermal tissues. Hidrotic and hypohidrotic ectodermal dysplasia are the two most common types of the disease. The typical oral features include malformed
L. Aldosari
semanticscholar +1 more source
Hoof nail deformity: a previously unknown hereditary nail malformation
British Journal of Dermatology, 2013G.W. Jung, T.G. Salopek
openaire +1 more source
Possible trisomy 1q25→1q32 in a malformed girl with a de novo insertion in 1q
Human Genetics, 1979A. Schinzel
semanticscholar +1 more source
Pycnodysostosis: the disease of Henri de Toulouse-Lautrec
European Journal of Orthopaedic Surgery & Traumatology, 2018K. Markatos +3 more
semanticscholar +1 more source