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Dermatology online journal, 07/2019, Volume 25, Issue 7
Juvenile hyaline fibromatosis is a recessive autosomal hereditary disorder characterized by abnormal growth of hyalinized fibrous tissue. Its clinical... 
Contracture - drug therapy | Young Adult | Hyalinosis, Systemic - diagnosis | Humans | Hyalinosis, Systemic - pathology | Male | Disease Progression | Hyalinosis, Systemic - therapy | Skin - pathology
Journal Article
Journal of Veterinary Diagnostic Investigation, ISSN 1040-6387, 9/2017, Volume 29, Issue 5, pp. 691 - 695
Journal Article
Journal Article
Nature Communications, ISSN 2041-1723, 06/2017, Volume 8, Issue 1, p. 15861
Loss-of-function mutations in capillary morphogenesis gene 2 (CMG2/ANTXR2), a transmembrane surface protein, cause hyaline fibromatosis syndrome (HFS), a... 
INFANTILE SYSTEMIC HYALINOSIS | FIBROSIS | SERINE PROTEINASES | TGF-BETA | MULTIDISCIPLINARY SCIENCES | MOUSE | CAPILLARY MORPHOGENESIS PROTEIN-2 | ANTHRAX TOXIN | RECEPTOR | MUTATIONS | EXPRESSION
Journal Article
EMBO Molecular Medicine, ISSN 1757-4676, 04/2011, Volume 3, Issue 4, pp. 208 - 221
Journal Article
Molecular medicine reports, 10/2018, Volume 18, Issue 4, p. 4004
Hyaline fibromatosis syndrome (HFS; MIM 228600) is a rare autosomal recessive disorder characterized by the abnormal growth of hyalinized fibrous tissue at... 
DNA Mutational Analysis | Base Sequence | Humans | Asian Continental Ancestry Group - genetics | Hyalinosis, Systemic - pathology | Male | Mutation - genetics | Child | Hyalinosis, Systemic - genetics | Receptors, Peptide - genetics | Syndrome | Hyalinosis, Systemic - diagnostic imaging
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 03/2016, Volume 91, Issue 2, pp. 226 - 229
Hyaline fibromatosis syndrome is the current name for clinical manifestations of diseases previously known as "infantile systemic hyalinosis" and "juvenile... 
Fibroma | Mutation | Skin: Skin manifestations | Gingival hypertrophy | GRADING SYSTEM | SYSTEMIC HYALINOSIS | DERMATOLOGY | Biopsy | Humans | Hyalinosis, Systemic - pathology | Child, Preschool | Female | Male | Early Diagnosis | Hyalinosis, Systemic - therapy | Skin - pathology | Case Report
Journal Article
Zdorovʹe Rebenka, ISSN 2224-0551, 05/2015, Volume 10, Issue 4.64, pp. 111 - 117
Infantile systemic hyalinosis — one of the forms of systemic hyaline fibromatosis — is a rare, fatal progressive disease with autosomal recessive inheritance,... 
children | hyalinosis
Journal Article
12/2008
We describe here a three year-old girl with classic clinical and histological features of juvenile hyaline fibromatosis. We found a history of similar skin... 
Allelic disorders | Hyalinosis | Fibromatosis
Web Resource
Journal of the European Academy of Dermatology and Venereology, ISSN 0926-9959, 05/2016, Volume 30, Issue 5, pp. 902 - 904
Journal Article
Journal of Medical Case Reports, ISSN 1752-1947, 09/2014, Volume 8, Issue 1, pp. 291 - 291
Juvenile hyaline fibromatosis and infantile systemic hyalinosis are variants of the same autosomal recessive syndrome; hyaline fibromatosis syndrome,... 
Infantile systemic hyalinosis | Hyaline fibromatosis syndrome | CMG2 | Hyalinosis, Systemic - diagnosis | Diagnosis, Differential | Gene Deletion | Humans | Genetic Association Studies - methods | Male | Child | Hyalinosis, Systemic - genetics | Receptors, Peptide - genetics | Syndrome | Health aspects | Medical genetics
Journal Article