Results 1 to 10 of about 273,607 (146)

Early Recognition of Infantile Systemic Hyalinosis in a Palestinian Infant: A Case Report. [PDF]

Clin Case Rep
ABSTRACT Infantile systemic hyalinosis should be suspected in infants with contractures, skin changes, and diarrhea in consanguineous families. Early recognition allows timely genetic testing, supportive care, and counseling, improving family outcomes despite poor prognosis.
Jarrar L, Mutan S, Malhis L, Mashni A, Ajlone A, Zaid M, Abuaisha S.   +6 more
europepmc   +2 more sources

Anti-Proliferative Effects of Resveratrol on Gingival Fibroblasts Derived From Amlodipine-Induced Gingival Overgrowth. [PDF]

J Periodontal Res
Kara B, Saygun NI, Köse Özkan C, Özgül Slezovic M, Serdar MA, Elçi MP, Kantarci A.   +6 more
europepmc   +1 more source

Very Rare Case of Hyaline Fibromatosis Syndrome Successfully Treated with Surgical Excision and Review of Literature. [PDF]

Arch Plast Surg
Jung YU, Kim BJ, Kim EH.
europepmc   +1 more source

Infantile Systemic Hyalinosis: A Familiar Symptom Unveiling an Unusual Disease. [PDF]

Cureus
Nayek S, Sandhu A, Kumar A, Malik S.
europepmc   +1 more source

Zimmermann-Laband syndrome-associated hereditary gingival fibromatosis.

J Indian Soc Periodontol, 2023
Kshirsagar JT, Dharani K, Thangavel P.
europepmc   +1 more source

Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation. [PDF]

Cureus
Goswami D, Rai R, Jain P, Goswami PP.
europepmc   +1 more source

Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis. [PDF]

Am J Hum Genet, 2003
Dowling O, Difeo A, Ramirez MC, Tukel T, Narla G, Bonafe L, Kayserili H, Yuksel-Apak M, Paller AS, Norton K, Teebi AS, Grum-Tokars V, Martin GS, Davis GE, Glucksman MJ, Martignetti JA.   +15 more
europepmc   +1 more source

Fibronectin 1 (<i>FN1</i>)-rearranged Mesenchymal Neoplasms: An Updated Review. [PDF]

Cancer Genomics Proteomics
Nishio J, Chijiiwa Y, Shinohara Y, Aoki M, Koga K.   +4 more
europepmc   +1 more source

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. [PDF]

Am J Hum Genet, 2003
Hanks S, Adams S, Douglas J, Arbour L, Atherton DJ, Balci S, Bode H, Campbell ME, Feingold M, Keser G, Kleijer W, Mancini G, McGrath JA, Muntoni F, Nanda A, Teare MD, Warman M, Pope FM, Superti-Furga A, Futreal PA, Rahman N.   +20 more
europepmc   +1 more source

Juvenile hyaline fibromatosis.

JPMA. The Journal of the Pakistan Medical Association, 1991
T S, Haroon, Z, Zaidi
openaire   +1 more source