Polyhydramnios
Mostrando 1-12 de 14 artigos, teses e dissertações.
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1. A two-year follow-up of asfotase alfa replacement in a patient with hypophosphatasia: clinical, biochemical, and radiological evaluation
SUMMARY Hypophosphatasia (HPP) is a rare disease with a high mortality rate in its severe forms. It is caused by mutations within the gene encoding the tissue-nonspecific alkaline phosphatase (TNSALP), an enzyme responsible for bone mineralization. In 2015, the Food and Drug Administration approved the use of asfotase alfa, the first medication showing benef
Arch. Endocrinol. Metab.. Publicado em: 2020-10
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2. Treatment of insomnia with repetitive transcranial magnetic stimulation (rTMS) in a patient with posttraumatic stress disorder (PTSD)
SUMMARY Hypophosphatasia (HPP) is a rare disease with a high mortality rate in its severe forms. It is caused by mutations within the gene encoding the tissue-nonspecific alkaline phosphatase (TNSALP), an enzyme responsible for bone mineralization. In 2015, the Food and Drug Administration approved the use of asfotase alfa, the first medication showing benef
Arch. Clin. Psychiatry (São Paulo). Publicado em: 2020-10
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3. Analysis of obstetrical and neonatal outcomes in pregnant women with end-stage renal disease on chronic dialysis / Análise dos resultados obstétricos e perinatais das gestantes com insuficiência renal crônica em terapia dialítica
Pregnancy in women with end-stage renal disease (ESRD) requiring chronic dialysis is a rare event. After the 90 decade, there was an increased number of cases reporting success in these pregnancies. During the period of 1999 to 2007 we studied the obstetrical and perinatal outcomes of 30 pregnancies in 27 patients on dialysis, with an average age of 30.4 ±
Publicado em: 2009
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4. "A relação entre o perfil glicêmico materno e o índice de líquido amniótico em gestações complicadas pelo diabetes mellitus" / Association between glycemic control and amniotic fluid index in pregnancies complicated by diabetes mellitus
To examine the association between glycemic control and amniotic fluid volume sixty pregnancies with pre-existing diabetes were examined. Amniotic fluid index (AFI) was evaluated weekly after 27 weeks of gestation and self-monitoring blood glucose levels (expressed as mean blood glucose levels and percentage of abnormal values) were recorded the week before
Publicado em: 2006
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5. Alterações ultrassonógráficas de 2° e 3° trimestres observadas em 143 fetos submetidos ao estudo cromossômico e acompanhados no Centro de Medicina Fetal / UFMG
Purpose: To describe the ultrasonographic findings observed in 143 fetuses, associating them with the main chromosomal anomalies and verifying if there is a typical ultrasonographic alteration that could be related to a particular chromosomopathy. Method: A retrospective and descriptive study was carried out including 143 fetuses with ultrasonographic abnorm
Publicado em: 2003
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6. Medical genetics: advances in brief: Fumarase deficiency: two siblings with enlarged cerebral ventricles and polyhydramnios in utero
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7. Congenital hypothyroidism, spiky hair, and cleft palate.
Two brothers are described with athyroidal hypothyroidism, spiky hair, choanal atresia, cleft palate, and bifid epiglottis. Polyhydramnios was present in the third trimester of each pregnancy. These abnormalities appear to represent a new syndrome.
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8. Raised alpha-fetoprotein levels in amniotic fluid and maternal serum associated with distension of the fetal bladder caused by absence of urethra.
Raised alpha-fetoprotein concentrations were found at 29 and 30 weeks' gestation in the amniotic fluid and maternal serum of a woman who presented in her seventh pregnancy with apparent polyhydramnios. The fetus had multiple abnormalities including gross distension of the bladder resulting from absence of the urethra, intestinal artresia, and a congenital he
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9. Mosaic partial trisomy 17q2.
Examination of an infant born after prenatal diagnosis of mosaic partial trisomy 17q2 showed the unique phenotypic features of this chromosomal abnormality, that is, frontal bossing, large mouth, brachyrhizomelia, and hexadactyly. Amniocentesis was performed because of polyhydramnios and ultrasound diagnosis of fetal craniofacial dysmorphology and rhizomelic
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10. The Baller-Gerold syndrome.
A case of severe craniosynostosis-radial aplasia (Baller-Gerold) syndrome is described in a newborn male, following a pregnancy complicated by polyhydramnios and intrauterine growth retardation. Death occurred after two hours owing to a prolonged apnoeic spell. Extensive agenesis of the frontal and parietal bones, resulting in a very large fontanelle, in add
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11. Subhuman Primate Pregnancy Complicated by Streptozotocin-Induced Diabetes Mellitus
Polydipsia, polyuria, polyphagia, and glucosuria followed the administration of streptozotocin to 6 nonpregnant and 15 pregnant monkeys (Macaca mulatta) in the first trimester of pregnancy. The diabetogenic action of the drug was also reflected in an induced but variable deterioration in maternal intravenous glucose tolerance and a marked attenuation of mate
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12. Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniques.
A patient was referred for amniocentesis because of advanced maternal age and polyhydramnios. The fetal karyotype was a mosaic 46,XX,del(18)(p11.1)/46,XX,-18,+i(18q)de novo. The deletion appeared to encompass the whole short arm as evidenced by G banding and in situ hybridisation. However, telomere sequences were found on both ends of the deleted chromosome