Перегляд вихідного коду сторінки New Perspective Around GUCY1B3 Just Made available

This family may represent one of the first descriptions of familial inheritance and evolving phenotype in MSBD. The evidence for male�Cmale transmission would support the existence of an autosomal mechanism of inheritance for a novel form of MSBD with characteristic syndromic features. ? 2012 Wiley Periodicals, Inc. ""Wiedemann�CRautenstrauch syndrome (WRS) is a rare autosomal recessive disorder that includes premature aging phenotype at birth. The condition is also known as a neonatal progeroid syndrome. Up to now only a few published case reports have been documented. The syndrome is characterized by progeroid appearance, decreased subcutaneous fat, hypotrichosis, macrocephaly, and in some natal teeth. We describe a new patient with features of bilaterally pelvicalyceal ectasia and partial syndactyly on 2th and 3th toes, not previously described, to our knowledge. ? 2012 Wiley Periodicals, Inc. ""Spina [http://www.selleckchem.com/products/pexidartinib-plx3397.html selleck chemical] bifida, a neural tube closure defect (NTD) involving the posterior portion of what will ultimately give rise to the spinal cord, is one of the most common and serious birth defects. The etiology of spina bifida is thought [http://www.selleckchem.com/products/BKM-120.html this website] to be multi-factorial and involve multiple interacting genes and environmental factors. The causes of this congenital malformation remain largely unknown. However, several candidate genes for spina bifida have been identified in lower vertebrates, including the planar cell polarity (PCP) genes. We used data from a case�Ccontrol study conducted in California to evaluate the association between variation within several key PCP genes and the risk of spina bifida. The PCP genes included in this study were the human homologs of the Xenopus genes Flamingo, Strabismus, Prickle, Dishevelled, and Scrib, two of the homologs of Xenopus Wnt genes, WNT5A and WNT11, and two of the homologs of Xenopus Frizzled, FZD3 and FZD6. None of the 172 SNPs that were evaluated were significantly associated with spina bifida in any racial/ethnic group after correction for multiple testing. However, several SNPs in the PRICKLE2 gene had unadjusted P-value [http://en.wikipedia.org/wiki/GUCY1B3 GUCY1B3] gene may potentially modify the risk of spina bifida and deserves further investigation. ? 2010 Wiley-Liss, Inc. ""We report on clinical and molecular findings of a 15-year-old female referred to our genetics clinic for a diagnostic evaluation due to mild developmental delay, submucosal cleft palate, and seizure disorder. Chromosomal microarray technology revealed a cancer predisposition due to a terminal deletion on chromosome 19p that includes the tumor suppressor gene STK11. In addition to abnormal lip pigmentation on exam, further diagnostic workup with upper and lower gastrointestinal screening confirmed polyps consistent with Peutz�CJeghers syndrome.