Cargando…

Juvenile Hyaline Fibromatosis: A 10-year Follow-up

Juvenile hyaline fibromatosis (JHF) is a rare hereditary disease with an autosomal recessive transmission. JHF is characterized by papulonodular skin lesions, osteolytic bone lesions, flexural joint contractures, and gingival hyperplasia and usually diagnosed in infancy or early childhood. JHF is th...

Descripción completa

Detalles Bibliográficos
Autores principales:	Baltacioglu, Esra, Guzeldemir, Esra, Sukuroglu, Erkan, Yildiz, Kadriye, Yuva, Pinar, Aydin, Güven, Karacal, Naci
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363149/ https://www.ncbi.nlm.nih.gov/pubmed/28400645 http://dx.doi.org/10.4103/ijd.IJD_166_16

Ejemplares similares

Juvenile Hyaline Fibromatosis
por: Park, Kyung Tae, et al.
Publicado: (2010)

JUVENILE HYALINE FIBROMATOSIS
por: Krishnamurthy, Jayashree, et al.
Publicado: (2011)

Juvenile Hyaline Fibromatosis
por: Karande, Vikram, et al.
Publicado: (2018)

Protein carbonyl levels in serum, saliva and gingival crevicular fluid in patients with chronic and aggressive periodontitis
por: Baltacioglu, Esra, et al.
Publicado: (2019)

Peri-implant plastic surgery techniques to hard and soft tissue augmentation in implant rehabilitation
por: Baltacioğlu, Esra, et al.
Publicado: (2017)

Overlapping Hyaline Fibromatosis Syndrome: A Rare Case of Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
por: Oswal, Rupal M, et al.
Publicado: (2022)

Juvenile hyaline fibromatosis: A rare genetic disorder
por: Tripathy, Sumita, et al.
Publicado: (2020)

Combined Soft and Hard Tissue Peri-Implant Plastic Surgery Techniques to Enhance Implant Rehabilitation: A Case Report
por: Baltacıoğlu, Esra, et al.
Publicado: (2014)

Atypical Presentation of Lip Nodules in Clinically Diagnosed Juvenile Hyaline Fibromatosis
por: Khoo, Ee Theng, et al.
Publicado: (2023)

The diagnostic challenge of juvenile hyaline fibromatosis, a case report with literature reviews
por: Ahmed, Ronak S., et al.
Publicado: (2022)

Imaging manifestations of juvenile hyaline fibromatosis: a case report and literature review
por: Yu, Jinfen, et al.
Publicado: (2022)

Hyaline fibromatosis syndrome: cutaneous manifestations
por: Marques, Silvio Alencar, et al.
Publicado: (2016)

Juvenile Hyaline Fibromatosis: Literature Review and a Case Treated With Surgical Excision and Corticosteroid
por: Braizat, Omar, et al.
Publicado: (2020)

Multiple Scalp Tumors in Juvenile Hyaline Fibromatosis with Antxr-2 Mutation in a Family
por: Mendiratta, Vibhu, et al.
Publicado: (2021)

Juvenile hyaline fibromatosis: a rare oral disease case report and literature review
por: Xia, Liang, et al.
Publicado: (2021)

Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation
por: Choochuen, Pongsakorn, et al.
Publicado: (2022)

Hyaline Fibromatosis Syndrome: A Rare Inherited Disorder
por: Mantri, Meeta Dipak, et al.
Publicado: (2016)

Gingival Hypertrophy in a Child with Hyaline Fibromatosis Syndrome
por: Knežević, Predrag, et al.
Publicado: (2020)

Multisystemic Manifestations of Hyaline Fibromatosis Syndrome: Implications for Diagnosis and Management
por: Albusta, Noor, et al.
Publicado: (2023)

Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation
por: Härter, Bettina, et al.
Publicado: (2020)

Anesthetic Management of a Patient With Juvenile Hyaline Fibromatosis: A Case Report Written With the Assistance of the Large Language Model ChatGPT
por: Segal, Scott, et al.
Publicado: (2023)

Genetic, clinical and biochemical characterization of a large cohort of patients with hyaline fibromatosis syndrome
por: Cozma, Claudia, et al.
Publicado: (2019)

Enhanced Collagen Deposition in the Duodenum of Patients with Hyaline Fibromatosis Syndrome and Protein Losing Enteropathy
por: van Rijn, Jorik M., et al.
Publicado: (2020)

Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome
por: Haidar, Zahraa, et al.
Publicado: (2017)

Systemic moxifloxacin vs amoxicillin/metronidazole adjunct to non-surgical treatment in generalized aggressive periodontitis
por: Guzeldemir-Akcakanat, Esra, et al.
Publicado: (2015)

Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report
por: Cherkaoui Jaouad, Imane, et al.
Publicado: (2014)

Erratum to: Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome
por: Haidar, Zahraa, et al.
Publicado: (2017)

The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series
por: Youssefian, Leila, et al.
Publicado: (2018)

CMG2/ANTXR2 regulates extracellular collagen VI which accumulates in hyaline fibromatosis syndrome
por: Bürgi, Jérôme, et al.
Publicado: (2017)

A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in ANTXR2 Gene
por: Park, Chan Seong, et al.
Publicado: (2019)

Juvenile Localized Scleroderma with Hyaline Deposits in the Renal Arteriole
por: Tabata, Nobuko, et al.
Publicado: (2018)

Hyaline Fibromatosis Syndrome inducing mutations in the ectodomain of anthrax toxin receptor 2 can be rescued by proteasome inhibitors
por: Deuquet, Julie, et al.
Publicado: (2011)

Hypercalcemia as a rare presentation of hyaline fibromatosis syndrome from different Sudanese families: two case reports
por: Ismail, Mariam M., et al.
Publicado: (2023)

Safety and efficacy of flow diverter stents in the treatment of middle cerebral artery aneurysms: a single-center experience and follow-up data
por: Soydemir, Efe, et al.
Publicado: (2023)

Hyaline fibromatosis syndrome with a novel 4.41‐kb deletion in ANTXR2 gene: A case report and literature review
por: Zhu, Yunqian, et al.
Publicado: (2022)

Juvenile fibromatosis of the temporomandibular joint: A rare case report
por: Basha, Mohammed Salman, et al.
Publicado: (2014)

A minimally invasive technique for the management of severely fluorosed teeth: A two-year follow-up
por: Yildiz, Gul, et al.
Publicado: (2013)

Hereditary gingival fibromatosis and its management: 2-year follow-up
por: Tripathi, Amitandra Kumar, et al.
Publicado: (2014)

Aggressive juvenile fibromatosis of the paranasal sinuses: case report and brief review
por: Lakhan, Shaheen E, et al.
Publicado: (2008)

Hyaline fibromatosis syndrome: a case presenting with gingival enlargement as the only clinical manifestation and a report of two new mutations in the ANTXR2 gene
por: Liu, Yiying, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_mderhcg12d9ednl47cugec3tca