Gingival fibromatosis combined with cherubism

Ramon, Yochanan; Berman, Wulfred; Bubis, José

doi:10.1016/0030-4220(67)90416-1

Cited by 92 publications

(54 citation statements)

References 18 publications

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“…It may be sporadic or inherited as an autosomal dominant trait and occurs between one in 1000-2500 [30][31][32]. The Ramon syndrome consists of mental deficiency, epilepsy, cherubism, gingival fibromatosis, hypertrichosis, stunted growth and juvenile rheumatoid arthritis [33,34]. The rare cases with NF1 association have shown multiple mutations (NF1, SH3BP2, PTPN11) [35,36].…”

Section: Fibrous Dysplasiamentioning

confidence: 99%

Benign Fibro-Osseous Lesions of the Craniofacial Complex A Review

Eversole

El‐Mofty

2008

Head and Neck Pathol

275

357

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Benign fibro-osseous lesions of the craniofacial complex are represented by a variety of disease processes that are characterized by pathologic ossifications and calcifications in association with a hypercellular fibroblastic marrow element. The current classification includes neoplasms, developmental dysplastic lesions and inflammatory/reactive processes. The definitive diagnosis can rarely be rendered on the basis of histopathologic features alone; rather, procurement of a final diagnosis is usually dependent upon assessment of microscopic, clinical and imaging features together. Fibrous dysplasia and osteitis deformans constitute two dysplastic lesions in which mutations have been uncovered. Other dysplastic bone diseases of the craniofacial complex include florid osseous dysplasia, focal cemento-osseous dysplasia and periapical cemental dysplasia, all showing a predilection for African descent individuals; although no specific genetic alterations in DNA coding have yet to be uncovered and most studies have been derived from predominant high African descent populations. Ossifying fibromas are neoplastic lesions with four subtypes varying with regard to behavior and propensity for recurrence after surgical excision. The clinicopathologic and molecular features of this unique yet heterogeneous group of diseases are reviewed.

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Section: Fibrous Dysplasiamentioning

confidence: 99%

Benign Fibro-Osseous Lesions of the Craniofacial Complex A Review

Eversole

El‐Mofty

2008

Head and Neck Pathol

275

357

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“…HGF'nin men tal re tar das yon, epi lep si, hi per tri koz, Zim mermann-La band, Ra mon, Cross sen dro mu gi bi durum lar la bir lik te gö rü le bil di ği bil di ril miş tir. 1,3,7,19 Fa kat bu ol gu çalışmasında in ce le nen hiç bir ai le bire yin de her han gi bir ek bul gu ya rast lan ma dı. Tüm ai le bi rey le ri men tal açı dan nor mal ve sis te mik olarak sağ lık lı idi.…”

Section: Tar Tiş Maunclassified

“…Cop yright © 2015 by Tür ki ye Kli nik le ri OLGU SUNUMU la rı nın bir bul gu su ola rak da or ta ya çı ka bi lir. [6][7][8] Di ş e ti bü yü me le ri ba zen je ne ra li ze olup her iki çe nede hem buk kal hem de lin gu al böl ge yi et ki le yebil mek te, ba zen de lo ka li ze olup sa de ce mak sil ler tü ber böl ge si, man di büler mo lar la rın buk kal böl-ge si ve ya man di büler ke ser le rin la bi al böl ge si gi bi özel bir böl ge de bu lu na bil mek te dir. 9,10 Diş ler radyog ra fik ola rak ke mik se vi ye si üze rin de sür müş gö-rün me si ne rağ men ağız da hiç sür me miş ya da kıs men sür müş ola rak gö rü ne bi lir.…”

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Hereditary Gingival Fibromatosis: Report of Two Cases

Meşeli¹,

Kati²,

Kuru³

2015

Turkiye Klinikleri J Dental Sci

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“…Although cherubism appears to be inherited as an autosomal dominant trait with 70% in females and 90% in males, other pattern of inheritance and association with syndromes has been reported [8][9][10]. Around puberty the condition begins to regress until by 30 years of age, when lesions frequently are not detectable.…”

Section: Review Of the Literaturementioning

confidence: 99%

Cherubism: Case Report with Review of Literature

Mehrotra

Kesarwani

Nandlal

2011

J. Maxillofac. Oral Surg.

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Cherubism is a rare hereditary fibro-osseous lesion characterized by painless expansion of jaws in childhood and is known to regress without treatment after puberty. Wait and watch approach has been advocated by many authors. The disease starts early in life manifesting itself fully in the second decade of life and is almost regressed in the third decade. Here, we report two cases of cherubism with clinico-radiographic presentation of its classical features in their third and fourth decade of life respectively and review the literature.

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Gingival fibromatosis combined with cherubism

Cited by 92 publications

References 18 publications

Benign Fibro-Osseous Lesions of the Craniofacial Complex A Review

Benign Fibro-Osseous Lesions of the Craniofacial Complex A Review

Hereditary Gingival Fibromatosis: Report of Two Cases

Cherubism: Case Report with Review of Literature

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