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|Type:||Artigo de periódico|
|Title:||Identification of 2 Novel ANTXR2 Mutations in Patients With Hyaline Fibromatosis Syndrome and Proposal of a Modified Grading System|
Raposo-Amaral, Cassio E.
Stelini, Rafael F.
Buzzo, Celso L.
Raposo-Amaral, Cesar A.
Hart, P. Suzanne
|Abstract:||Juvenile hyaline fibromatosis (JHF) and infantile systemic hyalinosis (ISH) are rare, autosomal recessive disorders of the connective tissue caused by mutations in the gene encoding the anthrax toxin receptor 2 protein (ANTXR2) located on chromosome 4q21. Characteristically, these conditions present with overlapping clinical features, such as nodules and/or pearly papules, gingival hyperplasia, flexion contractures of the joints, and osteolytic bone defects. The present report describes a pair of sibs and three other JHF/ISH patients whose diagnoses were based on typical clinical manifestations and confirmed by histopathologic analyses and/or molecular analysis. A comparison of ISH and JHF, additional thoughts about new terminology (hyaline fibromatosis syndrome) and a modified grading system are also included. (C) 2012 Wiley Periodicals, Inc.|
|Subject:||anthrax toxin receptor 2 protein|
capillary morphogenesis protein-2
hyaline fibromatosis syndrome
infantile systemic hyalinosis
juvenile hyaline fibromatosis
|Appears in Collections:||FCM - Artigos e Outros Documentos|
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