نتایج جستجو برای: consanguineous pakistani family

تعداد نتایج: 425994  

2014
Alexandros Onoufriadis Amelia Shoemark Mustafa M Munye Chela T James Miriam Schmidts Mitali Patel Elisabeth M Rosser Chiara Bacchelli Philip L Beales Peter J Scambler Stephen L Hart Jeannette E Danke-Roelse John J Sloper Sarah Hull Claire Hogg Richard D Emes Gerard Pals Anthony T Moore Eddie M K Chung Hannah M Mitchison

BACKGROUND Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous ciliopathy disorder affecting cilia and sperm motility. A range of ultrastructural defects of the axoneme underlie the disease, which is characterised by chronic respiratory symptoms and obstructive lung disease, infertility and body axis laterality defects. We applied a next-generation sequencing approach to ident...

Abdul Khaliq Naveed Fatima Qaiser Muhammad Jawad Yousaf Seyyedha Abbas, Shakir Khan, Suhail Razak Zahid Azeem

Objective(s): Genetic analysis of two consanguineous Pakistani families with localized autosomal recessive hypotrichosis was performed with the goal to establish genotype-phenotype correlation. Materials and Methods: Genomic DNA extraction had been done from peripheral blood samples. Extracted DNA was then subjected to PCR (polymerase chain reaction) for amplification. Linkage analysis was perf...

Journal: :Journal of medical genetics 1988
A Darr B Modell

An enquiry answered by 100 randomly selected British Pakistani mothers in the postnatal wards of two hospitals in West Yorkshire showed that 55 were married to their first cousins, while in only 33 cases had their mother been married to her first cousin. This suggests an increasing rate of consanguineous marriage in this relatively small group, by contrast with the decreasing rate observed in s...

Journal: :Journal of medical genetics 1993
A Curtis R J Richardson J Boohene A Jackson R Nelson S S Bhattacharya

The occurrence of cystic fibrosis is very rare in the Asian population. Carriers of the mutations most commonly found in Caucasians were not detected in a large Asian population sample of almost 900 chromosomes. However, an affected Pakistani child born to consanguineous parents was further investigated and shown to be homozygous for the mutation S549N (G-->A). Molecular and clinical data are p...

Journal: :American journal of epidemiology 1998
C Stoltenberg P Magnus R T Lie A K Daltveit L M Irgens

To analyze the influence of consanguinity and maternal education on stillbirth and infant death for children born in Norway between 1967 and 1993, the authors studied 7,274 children of ethnic Pakistani origin and 1,431,055 children of Norwegian ethnic origin. Of these children, 31.0% of the Pakistani children and 0.1% of the Norwegian children had parents who were first cousins. Consanguinity i...

2011
Kwanghyuk Lee Saadullah Khan Muhammad Ansar Regie Lyn P. Santos-Cortez Wasim Ahmad Suzanne M. Leal

Mutations in the estrogen-related receptor beta (ESRRB) gene is the underlying cause of autosomal recessive nonsyndromic hearing impairment (ARNSHI) due to the DFNB35 locus which maps to 14q24.3. A genome scan of a large consanguineous Pakistani pedigree with ARNSHI established linkage with a maximum multipoint LOD score of 4.2 to the 14q24 region and the region of homozygosity contained the ES...

Journal: :Dermatology 2010
Mazen Kurban Muhammad Wajid Yutaka Shimomura Angela M Christiano

BACKGROUND Congenital insensitivity to pain (CIP) (OMIM 243000) is a rare autosomal-recessive disorder. Clinically, CIP is characterized by insensitivity to all modalities of pain except neuropathic pain, and recurrent injuries frequently go unnoticed. CIP is caused by mutations in the SCN9A gene encoding for the Na1.7 channel. METHODS We analyzed the DNA from members of a consanguineous Paki...

Journal: :Hong Kong medical journal = Xianggang yi xue za zhi 2013
Anthony C C Fu K L Hon Paul C L Choi

In July 2011, a 1.82-kg full-term male was delivered by caesarean section at a regional hospital. The parents were a consanguineous Pakistani couple and this was their firstborn. At birth, the baby exhibited generalised ruptured bullae (Fig 1), but there was no family history of any bullous disorder. The boy’s nails were not dystrophic. New blisters continued to develop spontaneously, without a...

Journal: :Molecular Vision 2008
Sabika Firasat S. Amer Riazuddin Shaheen N. Khan Sheikh Riazuddin

PURPOSE To identify the disease-causing mutations in three consanguineous Pakistani families with multiple members affected by primary congenital glaucoma. METHODS Blood samples were collected, and DNA was extracted. Linkage analysis for reported primary congenital glaucoma loci was performed using closely spaced polymorphic microsatellite markers on genomic DNA from affected and unaffected f...

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