Non syndromic gingival fibromatosis in a mild mental retardation child
نویسندگان
چکیده
منابع مشابه
A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation.
A female child with a terminal deletion on the long arm of chromosome 14, 46,XX,del(14)(q31.1), presented with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and a small haemangioma on the back. She was mildly mentally retarded. Only a few patients with a partial deletion of 14q (14q-) have been reported without consistent clinical findings. Although a clinical syndrome as...
متن کاملGenetics of non-syndromic autosomal recessive mental retardation.
Non-syndromic mental retardation is one of the most serious neurodevelopmental disorders, which has a serious impact not only on the affected individuals and their families but also on the health care system and society. Previously research has been more focused on the X-linked mental retardation and only recently studies have shown that non-syndromic autosomal recessive mental retardation is e...
متن کاملAetiology of mild mental retardation.
A clinical and family study was carried out in 169 children attending schools for the mildly mentally retarded in Southampton to assess the prevalence of recognised medical risk factors; 71 children (42%) had such risk factors. These were prenatal in 22, perinatal in 41, and postnatal in eight. Risk factors of possible, but less certain, significance were found in a further 63 children (37%). I...
متن کامل[Heterogeneity in gingival fibromatosis].
Five cases of familial and idiopathic gingival fibromatosis were reported. One case exhibited peculiar histologic features, which consisted of active growth of the fibroblastic cells. One hundred and ninety-six cases of gingival fibromatosis, whose clinical and/or pathologic findings were known, were collected from foreign literatures. The heterogeneity in gingival fibromatosis was discussed.
متن کاملGingival fibromatosis: a case report.
AIM Gingival Fibromatosis is characterised by a large increase in the gingival dimension which extends above the dental crowns, covering them partially or completely. The causes of the disease may have a genetic origin, in which case gingival hyperplasia may occur in isolation or be part of a syndrome, or acquired origin, which comes from specific drugs administered systemically. A form of ging...
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ژورنال
عنوان ژورنال: Contemporary Clinical Dentistry
سال: 2012
ISSN: 0976-237X
DOI: 10.4103/0976-237x.101096