Case reports of a new syndrome associating gingival fibromatosis and dental abnormalities in a consanguineous family.
about
FAM20A mutations can cause enamel-renal syndrome (ERS).Novel FAM20A mutations in hypoplastic amelogenesis imperfectaWhole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndromeGingival fibromatosis: clinical, molecular and therapeutic issuesHereditary gingival fibromatosis: clinical and ultrastructural features of a new family.Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutationsMinichromosome maintenance 2 and 5 expressions are increased in the epithelium of hereditary gingival fibromatosis associated with dental abnormalitiesFurther evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.Imaging evalution of the gingival fibromatosis and dental abnormalities syndromeImmunoexpression of α2-integrin and Hsp47 in hereditary gingival fibromatosis and gingival fibromatosis-associated dental abnormalities.Syndromes as they relate to periodontal disease.Amelogenesis imperfecta associated with dental follicular-like hamartomas and generalised gingival enlargement.Current concepts on gingival fibromatosis-related syndromes.Association of Amelogenesis Imperfecta and Bartter's Syndrome.Enamel renal syndrome with associated amelogenesis imperfecta, nephrolithiasis, and hypocitraturia: A case report.Typical Features of Amelogenesis Imperfecta in Two Patients with Bartter's Syndrome.Extensive Gingival Enlargement in Siblings: A case report.Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.Generalized pulp stones: report of a case with 6-year follow-up.Enamel-renal-gingival syndrome and FAM20A mutations.
P2860
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P2860
Case reports of a new syndrome associating gingival fibromatosis and dental abnormalities in a consanguineous family.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Case reports of a new syndrome ...... es in a consanguineous family.
@en
Case reports of a new syndrome ...... es in a consanguineous family.
@nl
type
label
Case reports of a new syndrome ...... es in a consanguineous family.
@en
Case reports of a new syndrome ...... es in a consanguineous family.
@nl
prefLabel
Case reports of a new syndrome ...... es in a consanguineous family.
@en
Case reports of a new syndrome ...... es in a consanguineous family.
@nl
P2093
P2860
P356
P1476
Case reports of a new syndrome ...... es in a consanguineous family.
@en
P2093
Hercílio Martelli-Júnior
Luis Antônio Nogueira Dos Santos
Marcelo Gonçalves Cavalcanti
Paulo Rogério Ferreti Bonan
Ricardo D Coletta
Suelleng Maria Cunha Santos
P2860
P304
P356
10.1902/JOP.2008.070520
P407
P577
2008-07-01T00:00:00Z