Results 111 to 120 of about 4,293 (240)

Tumoral calcinosis: a case report

The Turkish Journal of Pediatrics, 1999
Tumoral calcinosis is a rare disorder with the calcified masses in subcutaneous tissues. We report herein a nine-year-old girl, in whom the calcified lesions bilaterally involved the soft tissues in the anterior part of the knee joint.
I Ozkan, C Türeli, E Cullu, C Karaman, F Sendur, B Alparslan   +5 more
doaj  

Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey

JCRPE, 2019
Inactivating autosomal recessive mutations in fibroblast growth factor 23 (FGF23), klotho (KL) and polypeptide N-acetylgalactosaminotransferase 3 (GALNT3) genes lead to a rare disorder, hyperphosphatemic familial tumoral calcinosis (HFTC).
Rabia Miray Kışla Ekinci, Fatih Gürbüz, Sibel Balcı, Atıl Bişgin, Mehmet Taştan, Bilgin Yüksel, Mustafa Yılmaz   +6 more
doaj   +1 more source

TUMORAL CALCINOSIS [PDF]

American Journal of Roentgenology, 1971
I, Yaghmai, P, Mirbod
openaire   +2 more sources

Pilomatrixoma. Revisión de 179 casos [PDF]

, 2016
Presentamos un estudio sobre 179 casos de Pilomatrixoma recogidos en los archivos del Hospital General 'Vall d'Hebrón' de Barcelona, entre los años 1972 y 1988. Tumoración de presentación pediátrica, cerca del 50% de los casos se han observado en menores
Berini Aytés, Leonardo, García Jiménez, Angel, Gay Escoda, Cosme, Malet Hernández, Daniel   +3 more
core  

Acute tumoral calcinosis due to severe hyperphosphatemia in a maintenance hemodialysis patient [PDF]

, 2016
Keizo Nishime, Hiroki Takahashi
openalex   +1 more source

Renal Abnormalities During Calcinosis Primary Tumor [PDF]

, 2020
Primary tumour calcinosis is a rare condition of unknown etiopathogeny. They are transmitted in an autosomal dominant or recessive mode and predominate in the black race.
Lenga Loumingou, Ida Aurélie, Loumingou, Richard   +1 more
core   +1 more source

First report of hyperphosphatemic familial tumoral calcinosis due to homozygous GALNT3 mutation in a 16-year-old boy [PDF]

Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare disorder HFTC is caused by a loss of function in fibroblast growth factor 23 (FGF23), leading to increased phosphate levels in the body and calcium deposition.
Gupta, Sushil, Shukla, Ajay, Tignath, Gargi   +2 more
core   +2 more sources

Uremic tumoral calcinosis with atypical manifestation. Case report

, 2022
Arbey Aristizábal­-Alzate, John Fredy Nieto­-Ríos, Daniela Trujillo-Agudelo, Dahyana Cadavid-Aljure, Lina María Serna-­Higuita, Gustavo Adolfo Zuluaga-­Valencia   +5 more
openalex   +1 more source

Tumoral Lipo-Calcinosis [PDF]

Acta Orthopaedica Scandinavica, 1970
, Hartofilakidis-Garofalidi, A, Theodossiou, J, Matsoukas, C, Rigopoulos, B, Papathanassiou   +4 more
openaire   +2 more sources

Genetic diseases resulting from disordered FGF23/klotho biology [PDF]

, 2017
Econs, Michael J.
core   +1 more source