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Kyuang TP, Dong-Yeop C, Myung-Whun S. Juvenile hyaline fibromatosis. Clin Exp Otorhinolaryngol. 2010; 3:102-106
El-Kamah GY, Fong K, El-Ruby M, Afifi HH, Clements SE, Lai-Cheong JE, Amr K, El-Darouti M, McGrath JA. Spectrum of mutations in the ANTXR2 (CMG2) gene in infantile systemic hyalinosis and juvenile hyaline fibromatosis. Br J Dermatol. 2010; 163:208-234
Thomas JE, Moossavi M, Mehregan D. Juvenile hyaline fibromatosis: a case report and review of the literature. Int J Dermatol. 2004; 43:785-789
Hakki SS, Ataoglu T, Avunduk MC, Erdemli E, Gunhan O, Rahman N. Periodontal treatment of two siblings with juvenile hyaline fibromatosis. J Clin Periodontol. 2005; 32:1016-1021
El-Maaytah M, Jerjes W, Shah P, Upile T, Murphy C, Ayliffe P. Gingival hyperplasia associated with juvenile hyaline fibromatosis: a case report and review of literature. J Oral Maxillofac Surg. 2010; 68:2604-2608
Murray J. Three peculiar cases of molluscum fibrosum in children. Medico-Chirurg Trans. 1873; 38:235-253
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Nofal A, Sanad M, Assaf M, Nofal E, Nassar A, Almokadem S, Attwa E, Elmosalamy K. Juvenile hyaline fibromatosis and infantile systemic hyalinosis: a unifying term and a proposed grading system. J Am Acad Dermatol. 2009; 61:695-700

Juvenile hyaline fibromatosis: impact of periodontal care on quality of life and a patient perspective

From Volume 42, Issue 7, September 2015 | Pages 656-666

Authors

Zehra Yonel

BDS, MFDS RCS(Ed), FHEA, BDS, MFDS (RCS Edin) (RCS Eng), PGCert, MPH (Hons), PhD

Department of Periodontology, Birmingham Dental Hospital, St Chad's Queensway, Birmingham B4 6NN, UK

Articles by Zehra Yonel

Sabrina Parmar

BDS, MJDF RCS(Eng)

Specialty Dentist in Periodontology, Birmingham Dental Hospital, St Chad's Queensway, Birmingham B4 6NN, UK

Articles by Sabrina Parmar

Iain LC Chapple

FDS RCS, PhD

Department of Periodontology, Birmingham Dental Hospital, St Chad's Queensway, Birmingham B4 6NN, UK

Articles by Iain LC Chapple

Abstract

Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive inherited condition presenting early in life and characterized by the accumulation of hyaline-like tissue in the skin as well as various organs. Gingival overgrowth is a significant oral manifestation. This paper highlights how early and essential periodontal intervention may be necessary to improve mastication and subsequent weight gain, and to eliminate pain and improve the patient's quality of life. Here we highlight the key features of this condition and demonstrate how appropriate surgical management can have a significant impact on a patient‘s wellbeing.

CPD/Clinical Relevance: Juvenile hyaline fibromatosis has a significant impact on patient wellbeing and it is therefore important that clinicians are able to recognize the condition and ensure that patients receive appropriate care and management.

Article

Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive inherited condition. Impaired collagen synthesis is thought to be the major underlying mechanism behind JHF1, with mutation in the gene encoding the capillary morphogenesis protein 2 (ANTXR2/CMG2) implicated in the development of this disease.2

The condition is characterized clinically by the following features:

The oral complications of JHF extend to limited mouth opening due to joint contracture, difficulty eating and maintaining oral hygiene and a negative impact on speech due to the gingival overgrowth.

Approximately 70 cases of JHF have been reported in the literature to date5 and, owing to the rarity of the condition, debate regarding its exact pathogenesis is ongoing.

The condition was first described in 1873 by Murray, who described it as ‘Molluscum fibrosum’ in children’.1,6 Several terms have subsequently been used to describe the condition and, in 1972, Kitano et al first used the term ‘Juvenile hyaline fibromatosis’, which is the most commonly used term in the literature today.3,7

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