Consanguinity [NEW TOPIC PAGE]

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From PubMed Clinical Queries

PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas

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• Search PubMed Clinical Queries for "Consanguinity" 

Results: 5 of 928

• Studying the determinant factors leading to congenital heart disease in newborns.
  Arjmandnia M, Besharati M, Rezvan S.J Educ Health Promot. 2018; 7:53. Epub 2018 Apr 3.
• Risk factors and comorbidities in Brazilian patients with orofacial clefts.
  Silva HPVD, Arruda TTS, Souza KSC, Bezerra JF, Leite GCP, Brito MEF, Lima VMGDM, Luchessi AD, Bortolin RH, Ururahy MAG, et al.Braz Oral Res. 2018; 32:e24. Epub 2018 Apr 5.
• Reproductive health profile and circumcision of females in the Hali semi-urban region, Saudi Arabia: A community-based cross-sectional survey.
  Milaat WA, Ibrahim NK, Albar HM.Ann Saudi Med. 2018 Mar-Apr; 38(2):81-89.
• Phenotypic spectrum and responses to recombinant human IGF1 (rhIGF1) therapy in patients with homozygous intronic pseudoexon growth hormone receptor mutation.
  Chatterjee S, Shapiro L, Rose SJ, Mushtaq T, Clayton PE, Ten SB, Bhangoo A, Kumbattae U, Dias R, Savage MO, et al.Eur J Endocrinol. 2018 May; 178(5):481-489. Epub 2018 Mar 2.
• Effects of mating patterns on genealogical trees: Assessment of the high carrier rate of Familial Mediterranean Fever in rural Israeli districts.
  Levy O, Gath IN.J Theor Biol. 2018 Apr 14; 443:92-99. Epub 2018 Jan 31.

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This column displays citations filtered to a specific clinical study category and scope. These search filters were developed by Haynes RB et al. See more filter information.

Systematic Reviews

Results: 5 of 46

• The Prevalence of Phenylketonuria in Arab Countries, Turkey, and Iran: A Systematic Review.
  El-Metwally A, Yousef Al-Ahaidib L, Ayman Sunqurah A, Al-Surimi K, Househ M, Alshehri A, Da'ar OB, Abdul Razzak H, AlOdaib AN.Biomed Res Int. 2018; 2018:7697210. Epub 2018 Apr 18.
• Correction to: A meta-analysis of consanguinity and breast cancer.
  Wild JB, Hwang MJ, Jones G.Ir J Med Sci. 2018 Apr 25; . Epub 2018 Apr 25.
• A meta-analysis of consanguinity and breast cancer.
  Wild JB, Hwang MJ, Jones G.Ir J Med Sci. 2018 Mar 24; . Epub 2018 Mar 24.
• Allergy and immunology in Africa: Challenges and unmet needs.
  El-Gamal YM, Hossny EM, El-Sayed ZA, Reda SM.J Allergy Clin Immunol. 2017 Nov; 140(5):1240-1243. Epub 2017 Sep 27.
• The Most Common Comorbidities in Dandy-Walker Syndrome Patients: A Systematic Review of Case Reports.
  Stambolliu E, Ioakeim-Ioannidou M, Kontokostas K, Dakoutrou M, Kousoulis AA.J Child Neurol. 2017 Sep; 32(10):886-902. Epub 2017 Jun 21.

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This column displays citations for systematic reviews, meta-analyses, reviews of clinical trials, evidence-based medicine, consensus development conferences, and guidelines. See filter information or additional related sources.

Medical Genetics

Topic:AllDiagnosisDifferential DiagnosisClinical DescriptionManagementGenetic CounselingMolecular GeneticsGenetic Testing

Results: 5 of 8803

• Consanguinity increases the risk for aggressive periodontitis.
  Çalışır M.J Periodontal Res. 2018 Jun 26; . Epub 2018 Jun 26.
• Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India.
  Amritkumar P, Jeffrey JM, Chandru J, Vanniya S P, Kalaimathi M, Ramakrishnan R, Karthikeyen NP, Srikumari Srisailapathy CR.BMC Med Genet. 2018 Jun 19; 19(1):105. Epub 2018 Jun 19.
• Prevalence of hereditary cancer susceptibility syndromes in children with cancer in a highly consanguineous population.
  Jastaniah W, Aljefri A, Ayas M, Alharbi M, Alkhayat N, Al-Anzi F, Yassin F, Alkasim F, Alharbi Q, Abdullah S, et al.Cancer Epidemiol. 2018 May 30; 55:88-95. Epub 2018 May 30.
• The Prevalence of Phenylketonuria in Arab Countries, Turkey, and Iran: A Systematic Review.
  El-Metwally A, Yousef Al-Ahaidib L, Ayman Sunqurah A, Al-Surimi K, Househ M, Alshehri A, Da'ar OB, Abdul Razzak H, AlOdaib AN.Biomed Res Int. 2018; 2018:7697210. Epub 2018 Apr 18.
• Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case report.
  Stephen J, Nampoothiri S, Vinayan KP, Yesodharan D, Remesh P, Gahl WA, Malicdan MCV.BMC Med Genet. 2018 May 16; 19(1):80. Epub 2018 May 16.

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This column displays citations pertaining to topics in medical genetics. See more filter information.