Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 14 de 14
Filtrar
1.
Orphanet J Rare Dis ; 17(1): 100, 2022 03 03.
Artigo em Inglês | MEDLINE | ID: mdl-35241104

RESUMO

BACKGROUND: Individuals with pathogenic variants in SATB2 display intellectual disability, speech and behavioral disorders, dental abnormalities and often features of Pierre Robin sequence. SATB2 encodes a transcription factor thought to play a role in bone remodeling. The primary aim of our study was to systematically review the skeletal manifestations of SATB2-associated syndrome. For this purpose, we performed a non-interventional, multicenter cohort study, from 2017 to 2018. We included 19 patients, 9 females and 10 males ranging in age from 2 to 19 years-old. The following data were collected prospectively for each patient: clinical data, bone markers and calcium and phosphate metabolism parameters, skeletal X-rays and bone mineral density. RESULTS: Digitiform impressions were present in 8/14 patients (57%). Vertebral compression fractures affected 6/17 patients (35%). Skeletal demineralization (16/17, 94%) and cortical thinning of vertebrae (15/17) were the most frequent radiological features at the spine. Long bones were generally demineralized (18/19). The distal phalanges were short, thick and abnormally shaped. C-telopeptide (CTX) and Alkaline phosphatase levels were in the upper normal values and osteocalcin and serum procollagen type 1 amino-terminal propeptide (P1NP) were both increased. Vitamin D insufficiency was frequent (66.7%). CONCLUSION: We conclude that SATB2 pathogenic variants are responsible for skeletal demineralization and osteoporosis. We found increased levels of bone formation markers, supporting the key role of SATB2 in osteoblast differentiation. These results support the need for bone evaluation in children and adult patients with SATB2-associated syndrome (SAS).


Assuntos
Fraturas por Compressão , Proteínas de Ligação à Região de Interação com a Matriz , Fraturas da Coluna Vertebral , Fatores de Transcrição , Adolescente , Adulto , Biomarcadores , Densidade Óssea/genética , Osso e Ossos , Criança , Pré-Escolar , Estudos de Coortes , Feminino , Fraturas por Compressão/genética , Fraturas por Compressão/metabolismo , Fraturas por Compressão/patologia , Humanos , Masculino , Proteínas de Ligação à Região de Interação com a Matriz/genética , Proteínas de Ligação à Região de Interação com a Matriz/metabolismo , Estudos Prospectivos , Fraturas da Coluna Vertebral/genética , Fraturas da Coluna Vertebral/metabolismo , Fraturas da Coluna Vertebral/patologia , Síndrome , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismo , Adulto Jovem
2.
Rev Med Interne ; 38(1): 44-52, 2017 Jan.
Artigo em Francês | MEDLINE | ID: mdl-27349612

RESUMO

Nephrolithiasis is a very common (prevalence around 10 to 12% in France) and recurrent disorder. Nephrolithiasis is associated to chronic kidney disease and is responsible for 2 to 3% of cases of end-stage renal disease, mainly if it is associated to nephrocalcinosis or to a monogenic disorder (1.6% of nephrolithiasis in adults, among them 1% of cystinuria). To understand the underlying pathophysiological processes, stone analysis (morphology and using infrared spectrophotometry) as well as minimal biological assessment including urine crystal research are required. The calcic nephrolithiasis is the more frequent subtype (>80%). Its medical treatment relies on simple dietary rules: non-alkaline hyperdiuresis>2 liters/day, calcium intake normalization (1 gram per day divided between the three principal meals), normalization of sodium (6 to 7 grams per day) and protein intake (1g/kg of theoretical body weight/day), and eviction of foods rich in oxalate. In case of persistent hypercalciuria (>0.1mmol/kg of theoretical body weight/day on free diet), a thiazide diuretic can be started while being aware to correct iatrogenic decrease in plasma potassium and urine citrate excretion. Measurement of bone mineral density must systematically be performed in patients with high 24 h-urinary calcium excretion. The medical treatment of uric acid nephrolithiasis relies on alkaline hyperdiuresis (goal of urine pH: 6.2 to 6.8). The use of allopurinol is justified only if urine uric acid is over 4mmol/day. Thanks to a well-managed preventive medical treatment, one can expect to stop the activity of nephrolithiasis in more than 80% of cases, making it one of the most accessible renal pathologies to preventive medical treatment.


Assuntos
Cálculos Renais/etiologia , Cálculos Renais/prevenção & controle , Nefrolitíase/etiologia , Nefrolitíase/prevenção & controle , Adulto , Cálcio da Dieta/administração & dosagem , França/epidemiologia , Humanos , Cálculos Renais/epidemiologia , Falência Renal Crônica/complicações , Falência Renal Crônica/epidemiologia , Falência Renal Crônica/terapia , Nefrolitíase/epidemiologia , Fatores de Risco , Ácido Úrico/urina
3.
J Cyst Fibros ; 15(6): 825-833, 2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27289197

RESUMO

BACKGROUND: Body composition (BC) analysis based on bioelectrical impedance analysis (BIA) provides conflicting results. The purpose of the study was to validate an equation specific for young patients with cystic fibrosis (CF), describe their BC and investigate its association with lung function. METHODS: Fifty-four young CF patients were evaluated by BIA and dual X-ray absorptiometry (DXA). An empirically derived CF-specific equation for fat-free mass (FFM) estimation by BIA was elaborated after stepwise multivariate regression and the agreement between BIA and DXA was assessed by Bland-Altman plots. The association between BC and lung function was investigated by regression analysis. RESULTS: The mean difference between the BIA and DXA assessment was close to zero. A total of 22.5% of patients (n=9) presented a FFM z-score≤-2. They had a worse pulmonary function and diaphragmatic impairment. Among these 9 patients, 7 had a normal BMI z-score>-1. CONCLUSIONS: BIA, based on a CF-specific equation, is a reliable method for BC assessment and allows the identification of patients at risk of nutritional degradation and bad respiratory prognosis.


Assuntos
Composição Corporal , Fibrose Cística , Absorciometria de Fóton/métodos , Adolescente , Índice de Massa Corporal , Criança , Fibrose Cística/diagnóstico , Fibrose Cística/fisiopatologia , Impedância Elétrica , Feminino , França , Humanos , Masculino , Prognóstico , Estudos Prospectivos , Testes de Função Respiratória/métodos , Estatística como Assunto , Adulto Jovem
4.
Rev Med Interne ; 34(10): 605-13, 2013 Oct.
Artigo em Francês | MEDLINE | ID: mdl-23195909

RESUMO

For the past 40 years, primary hyperparathyroidism has been recognized as a common endocrine disease which is, most often, "non-symptomatic", without the occurrence of nephrolithiasis or osteitis fibrosa cystica. Our knowledge in the pathophysiology has increased largely and diagnosis of primary hyperparathyroidism is usually easy. The only radical treatment is surgery and the surgical indications have been codified by several consensus conferences. For patients who do not undergo surgery, prolonged medical monitoring is needed.


Assuntos
Hiperparatireoidismo Primário , Cálcio/metabolismo , Doenças Cardiovasculares/diagnóstico , Doenças Cardiovasculares/etiologia , Diagnóstico Diferencial , Procedimentos Cirúrgicos Endócrinos , Gastroenteropatias/diagnóstico , Gastroenteropatias/etiologia , Humanos , Hiperparatireoidismo Primário/complicações , Hiperparatireoidismo Primário/diagnóstico , Hiperparatireoidismo Primário/epidemiologia , Hiperparatireoidismo Primário/terapia , Transtornos Mentais/diagnóstico , Transtornos Mentais/etiologia , Doenças Musculares/diagnóstico , Doenças Musculares/etiologia , Neoplasias das Paratireoides/complicações , Neoplasias das Paratireoides/diagnóstico
5.
Ann Endocrinol (Paris) ; 69(6): 501-10, 2008 Dec.
Artigo em Francês | MEDLINE | ID: mdl-18804195

RESUMO

Knowledge about vitamin D has greatly improved during the last few years. Vitamin D cannot any more be considered as exclusively necessary to prevent ricket/osteomalacia. Its role in the prevention of some osteoporotic fractures in the elderly (in association with calcium nutrition) is now well demonstrated and many epidemiologic and laboratory data argue for a role in the prevention of several diseases or anomalies (cancer, auto-immune diseases, cardiovascular events, sarcopenia...). A few intervention studies confirming some of these effects also exist. Vitamin D status can easily be assessed by measuring serum 25 hydroxy vitamin D (25OHD) level. However, many experts have claimed that the population-based reference values for 25OHD are too low and that the cut-off value below which vitamin D insufficiency can be present is somewhere between 20 and 40 ng/mL with a clear tendency to target values above 30 ng/mL (75 nmol/L). The main consequences are that vitamin D insufficiency is highly frequent whereas the currently recommended supplementation doses are not sufficient.


Assuntos
Deficiência de Vitamina D/diagnóstico , Vitamina D/fisiologia , Vitaminas/fisiologia , Animais , Humanos , Sistema Imunitário/fisiologia , Músculo Esquelético/fisiologia , Neoplasias/fisiopatologia , Estado Nutricional/fisiologia , Vitamina D/sangue
6.
Arch Pediatr ; 8(5): 516-24, 2001 May.
Artigo em Francês | MEDLINE | ID: mdl-11396114

RESUMO

The near constancy of extracellular calcium concentration is required for the numerous physiological functions of extra- and intracellular calcium. This implies that any change in extracellular calcium concentration must be detected in order to allow the appropriate correction by the homeostatic systems. The identification and cloning of a calcium-sensing receptor (CaR), which is expressed in the plasma membrane of parathyroid cells as well as many other cell types, has been a major advance in the understanding of the mechanisms involved in the control of extracellular calcium concentration. In addition, it demonstrated that extracellular calcium concentration itself is the first informative hormone-like messenger in this system. CaR belongs to the C subfamily of seven transmembrane-spanning G protein-coupled receptors. Several inherited disorders in extracellular calcium homeostasis are due to both activating or inactivating mutations in CaR gene, strengthening the essential role of CaR in the control of calcium metabolism.


Assuntos
Cálcio/metabolismo , Erros Inatos do Metabolismo , Receptores de Superfície Celular/fisiologia , Cálcio/farmacocinética , Homeostase , Humanos , Hipercalcemia/fisiopatologia , Hiperparatireoidismo , Hipocalcemia/fisiopatologia , Glândulas Paratireoides/fisiologia , Mutação Puntual , Receptores de Detecção de Cálcio , Receptores de Superfície Celular/genética
7.
Nephrologie ; 21(6): 283-90, 2000.
Artigo em Francês | MEDLINE | ID: mdl-11117107

RESUMO

Primary hyperparathyroidism is the third most frequent endocrine disorder. The condition required for diagnosis is inappropriately elevated secretion of parathyroid hormone (PTH) with respect to calcemia. Most often, the disease is due to a parathyroid adenoma, i.e. a monoclonal benign parathyroid tumor, less often to a parathyroid hyperplasia. The main tumorogenic mechanisms currently proposed are a DNA rearrangement in the PTH locus (transposition of the PTH promoter upstream to Cyclin D1/PRAD 1 gene) and a mutation of the gene responsible for multiple endocrine neoplasia type I. The clinical presentation has strikingly evolved towards a milder, asymptomatic form, frequently diagnosed on systematic screenings. Though the mechanism of hypercalcemia is better understood, several hypothesis are still being considered about the regulation of tumoral PTH secretion: the role of the expression of calcium-receptor in parathyroid gland cells, vitamin D receptor and estrogen receptor polymorphisms, etc. Surgery is still advised for symptomatic forms of the disease, either because of a bone involvement, or because of an evolutive nephrolithiasis. In the near future, the new calcium-receptor agonists could be a relevant therapeutic approach.


Assuntos
Hiperparatireoidismo , Humanos , Hiperparatireoidismo/diagnóstico , Hiperparatireoidismo/epidemiologia , Hiperparatireoidismo/genética , Hiperparatireoidismo/terapia , Neoplasia Endócrina Múltipla Tipo 1/genética , Hormônio Paratireóideo/genética , Hormônio Paratireóideo/metabolismo
8.
Genitif ; 1(4): 31, 1979 Sep.
Artigo em Francês | MEDLINE | ID: mdl-12158286

RESUMO

PIP: In this very short but fiery and violent paper against abortion the author states that most women seeking abortion are actually lying to themselves, pretending they want something which, in reality, they do not want, i.e. an abortion. The laws regulating abortion in most countries are such that a woman is practically forbidden to make an independent decision, despite, or because of the number of counseling sessions and of meetings with doctors that she must go through. Radio, television, newspapers and magazines, friends and relatives, all contribute to make of abortion a run-of-the-mill operation, while it should be seen as scandal, and as the total negation of any maternal instinct.^ieng


Assuntos
Aborto Induzido , Meios de Comunicação de Massa , Comunicação , Serviços de Planejamento Familiar , Psicologia
11.
Contracept Fertil Sex (Paris) ; 6(1): 23-30, 1978 Jan.
Artigo em Inglês, Francês | MEDLINE | ID: mdl-12260438

RESUMO

PIP: Comparison of gynecoobestetrical sociological and psychological features of 220 clients for voluntary abortion (IVG) and 180 new clients for contraception during 1 year in a family planning center shows that IVG clients are generally younger, more often single, less educated, employed in tertiary sector, but with as many children when they are married. Economic conditions do not seem to be more decisive for abortion than for contraception. Absence more than failure of contraception is the case, though certain abortions appear caused by an activation of intrapersonal conflicts through contraception; the highest frequency of contraception antecedents is found among the women who use abortion for at least the 2nd time.^ieng


Assuntos
Aspirantes a Aborto , Comportamento Contraceptivo , Aceitação pelo Paciente de Cuidados de Saúde , Aborto Induzido , Fatores Etários , Anticoncepção , Educação , Serviços de Planejamento Familiar , Planejamento em Saúde , Paridade , Classe Social
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA