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1.
J Med Genet ; 60(2): 204-211, 2023 02.
Artigo em Inglês | MEDLINE | ID: mdl-35477554

RESUMO

BACKGROUND: Dyggve-Melchior-Clausen dysplasia (DMC) and Smith-McCort dysplasia (SMC types 1 and 2) are rare spondyloepimetaphyseal dysplasias with identical radiological findings. The presence of intellectual disability in DMC and normal intellect in SMC differentiates the two. DMC and SMC1 are allelic and caused by homozygous or compound heterozygous variants in DYM. SMC2 is caused by variations in RAB33B. Both DYM and RAB33B are important in intravesicular transport and function in the Golgi apparatus. METHODS: Detailed clinical phenotyping and skeletal radiography followed by molecular testing were performed in all affected individuals. Next-generation sequencing and Sanger sequencing were used to confirm DYM and RAB33B variants. Sanger sequencing of familial variants was done in all parents. RESULTS: 24 affected individuals from seven centres are described. 18 had DMC and 6 had SMC2. Parental consanguinity was present in 15 of 19 (79%). Height <3 SD and gait abnormalities were seen in 20 and 14 individuals, respectively. The characteristic radiological findings of lacy iliac crests and double-humped vertebral bodies were seen in 96% and 88% of the affected. Radiological findings became attenuated with age. 23 individuals harboured biallelic variants in either DYM or RAB33B. Fourteen different variants were identified, out of which 10 were novel. The most frequently occurring variants in this group were c.719 C>A (3), c.1488_1489del (2), c.1484dup (2) and c.1563+2T>C (2) in DYM and c.400C>T (2) and c.186del (2) in RAB33B. The majority of these have not been reported previously. CONCLUSION: This large cohort from India contributes to the increasing knowledge of clinical and molecular findings in these rare 'Golgipathies'.


Assuntos
Nanismo , Deficiência Intelectual , Osteocondrodisplasias , Humanos , Deficiência Intelectual/diagnóstico por imagem , Deficiência Intelectual/genética , Mutação , Osteocondrodisplasias/diagnóstico por imagem , Osteocondrodisplasias/genética , Nanismo/diagnóstico por imagem , Nanismo/genética
2.
Strabismus ; 25(1): 39-42, 2017 03.
Artigo em Inglês | MEDLINE | ID: mdl-28140732

RESUMO

INTRODUCTION: Surgically induced necrotizing scleritis (SINS) is a rare but serious disorder that can develop many years after strabismus surgery. It is generally treated with high-dose steroids or immunosuppression. CASE REPORT: We describe a patient with Varadi Papp syndrome and congenital fibrosis of the extraocular muscles, who developed surgically induced necrotizing scleritis a month after strabismus surgery and was successfully managed by oral vitamin C and topical N-acetylcysteine 10%. DISCUSSION: While SINS is conventionally treated with steroids/immunosuppression, a conservative approach may be tried in milder cases. The role of topical N-acetylcysteine in managing this complication needs to be explored.


Assuntos
Acetilcisteína/uso terapêutico , Fibrose/complicações , Sequestradores de Radicais Livres/uso terapêutico , Procedimentos Cirúrgicos Oftalmológicos/efeitos adversos , Oftalmoplegia/complicações , Síndromes Orofaciodigitais/complicações , Esclerite/etiologia , Estrabismo/cirurgia , Administração Tópica , Ácido Ascórbico/administração & dosagem , Criança , Humanos , Masculino , Músculos Oculomotores/cirurgia , Soluções Oftálmicas , Complicações Pós-Operatórias , Esclerite/tratamento farmacológico
3.
Diabetes Res Clin Pract ; 77(2): 269-79, 2007 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-17229484

RESUMO

India is experiencing an epidemic of Type 2 diabetes mellitus (DM) in young adults. This study reports the prevalence of glucose intolerance, and insulin profiles, and their relationship to lifestyle factors in 2218 young adults (aged 26-32 years; 997 urban, 1221 rural) in south India. They were drawn from a cohort of 10,691 individuals born during 1969-1973 in Vellore and nearby villages. Family history, socio-economic status, physical activity and tobacco and alcohol use were recorded. Oral glucose tolerance tests were performed for diagnosis (WHO recommendations). Insulin resistance and secretion were derived from plasma insulin concentrations. Median BMI was 20.0kg/m(2). The prevalence of Type 2 DM and impaired glucose tolerance (IGT) was higher in urban than in rural subjects (3.7% versus 2.1%, p=0.02; 18.9% versus 14.3%, p=0.002, respectively), while prevalence of impaired fasting glycaemia (IFG) was similar in urban and rural populations (3.8% versus 3.4%, p=0.04). Type 2 DM, IGT, IFG or higher insulin resistance and increment were associated with higher socio-economic status (more household possessions) and higher percentage body fat, body mass index and waist/hip ratio. Insulin increment was lower in men with higher alcohol consumption. Our data suggest high levels of glucose intolerance in young rural and urban adults highlighting an urgent need for preventive action to avert a public health catastrophe in India.


Assuntos
Diabetes Mellitus Tipo 2/epidemiologia , Intolerância à Glucose/epidemiologia , Adulto , Estudos de Coortes , Feminino , Morte Fetal/epidemiologia , Inquéritos Epidemiológicos , Humanos , Índia/epidemiologia , Insulina/sangue , Masculino , Estado Civil , Prole de Múltiplos Nascimentos/estatística & dados numéricos , Obesidade/epidemiologia , Sobrepeso , Gravidez , Prevalência , População Rural , População Urbana
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