Results 101 to 110 of about 273,607 (146)

Decoding the Mystery of Multiple Swellings and Joint Contractures: Hyaline Fibromatosis Syndrome.

Indian J Dermatol
Varshini C, Chidambaram AC, Babu RMD, Vidhyasagar K, Sagayaraj B.   +4 more
europepmc   +1 more source

Oral Pemphigus in Children and Adolescents: A Narrative Review of Published Case Reports. [PDF]

Reports (MDPI)
Fytros F, Dimitropoulou P, Charisi C, Pliaka D, Spantidakis N, Poulopoulos K, Fasoula M, Karagiannidis E, Poulopoulos A, Zisis V.   +9 more
europepmc   +1 more source

Investigating the Influence of ANTXR2 Gene Mutations on Protective Antigen Binding for Heightened Anthrax Resistance. [PDF]

Genes (Basel)
Archana CA, Sekar YS, Suresh KP, Subramaniam S, Sagar N, Rani S, Anandakumar J, Pandey RK, Barman NN, Patil SS.   +9 more
europepmc   +1 more source

Genetic Variants in the <i>TBC1D2B</i> Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis. [PDF]

Int J Mol Sci
Kularbkaew T, Thongmak T, Sandeth P, Daroontum T, Durward CS, Vittayakittipong P, Duke P, Iamaroon A, Kintarak S, Intachai W, Ngamphiw C, Tongsima S, Jatooratthawichot P, Cox TC, Ketudat Cairns JR, Kantaputra P.   +15 more
europepmc   +1 more source

Juvenile hyaline fibromatosis

, 2019
openaire   +1 more source

A case of juvenile hyaline fibromatosis

Journal of Dermatology, 2006
ABSTRACTJuvenile hyaline fibromatosis (JHF) is a rare, autosomally‐recessive disease characterized by papulonodular skin lesions, soft tissue masses, joint contractures, gingival hypertrophy and osteolytic bone lesions. Its onset is in infancy or early childhood. The most commonly affected sites are the nose, chin, ears, scalp, back and knees.
Savaş Yaylı, Sevgi BAHADIR, Kadriye Yıldız   +2 more
exaly   +4 more sources

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Juvenile hyaline fibromatosis

International Journal of Pediatric Otorhinolaryngology, 1995
A case of juvenile hyaline fibromatosis in a 7-year-old Asian boy is presented. This autosomal recessive inherited condition has not been described in the otolaryngology literature before. We demonstrate the benefits surgical intervention, for treatment of gingival hypertrophy, can bring to the patient and outline the other features of this rare ...
F Raafat
exaly   +3 more sources

Juvenile hyaline fibromatosis: a case report

International Journal of Pediatric Otorhinolaryngology, 2003
Juvenile hyaline fibromatosis (JHF) is a rare disease with autosomal recessive inheritance. It is characterized by papulonodular skin lesions which are painless but cosmetically unacceptable, and often disturb normal joint function. The nose, chin, ears, scalp, back, and knees are the most common affected sites.
Fazilet Kayaselçuk, Levent Naci Özlüoğlu, Fatma Çaylaklı   +2 more
exaly   +3 more sources

Juvenile hyaline fibromatosis

Journal of the American Academy of Dermatology, 1987
The literature recording cases of the rare juvenile hyaline fibromatosis is reviewed. Gingival enlargement is a regular feature of this entity. A case report and treatment of the gingival lesions are described, and the differential diagnosis and prognosis are discussed.
J G, Camarasa, A, Moreno
  +7 more sources