1.
BMJ Case Rep
; 20152015 Dec 18.
Article
in English
| MEDLINE
| ID: mdl-26682835
ABSTRACT
Juvenile hyaline fibromatosis (JHF) is a rare progressive autosomal recessive disease that is characterised by papulonodular skin lesions, soft tissue masses, joint contractures, gingival hypertrophy and osteolytic bone lesions. We present an 18-month-old boy with JHF. This case demonstrates that JHF should be considered in the differential diagnosis when multiple subcutaneous nodules are observed in the face, head and neck. Gum hypertrophy with palatal nodules is unusual in JHF.
Subject(s)
Gingival Hyperplasia/etiology , Hyaline Fibromatosis Syndrome/complications , Hyaline Fibromatosis Syndrome/diagnosis , Fibroma/etiology , Humans , Infant , Male , Skin Neoplasms/etiology
2.
Indian J Pediatr
; 81(5): 511, 2014 May.
Article
in English
| MEDLINE
| ID: mdl-24037479