نتایج جستجو برای: parental consanguinity

تعداد نتایج: 53108  

Journal: :Japanese journal of ophthalmology 1997
M Hayakawa K Fujiki A Kanai M Matsumura Y Honda H Sakaue M Tamai T Sakuma T Tokoro T Yura N Kubota S Kawano M Matsui M Yuzawa Y Oguchi K Akeo E Adachi T Kimura Y Miyake M Horiguchi K Wakabayashi N Ishizaka K Koizumi M Uyama N Ohba

A nationwide, multicenter study of typical retinitis pigmentosa (RP) was carried out in collaboration with 18 hospitals throughout Japan to obtain current information for genetic counseling. We analyzed the genetic heterogeneity of RP based on the parental consanguinity of 434 probands registered during a 6-month period in 1990. A gradual decline in the frequency of consanguineous marriage was ...

2016
Anamika Giri Gamze Guven Ebba Lohmann Javier Simón-Sánchez

Background: PLA2G6-associated neurodegeneration (PLAN) is a recessive neurodegenerative disorder characterized by three distinct phenotypes: infantile neuroaxonal dystrophy (INAD), atypical neuroaxonal dystrophy (atypical NAD), and PLA2G6-related dystonia–parkinsonism. Methods: A consanguineous index case from Turkey was diagnosed with early-onset Parkinsonism at the Istanbul Faculty of Medicin...

2005
P. Himabindu S. Vishnupriya K. P. Shravankumar Vittal V. Rao Shyam P. Sunder

Acid phosphatase is a polymorphic nonspecific orthophosphate monoesterase which catalyses the cleaving of phosphoric acid and subsequent breakdown of several monophosphoric esters under acidic pH conditions. Acid phosphatase has a physiologic function as a flavin mononucleotide phosphatase (FMN) and regulates the intracellular concentrations of flavin coenzymes that are electron carriers in the...

2016
Siti Aishah Abdul Wahab Yusnita Yakob Nor Azimah Abdul Azize Zabedah Md Yunus Leong Huey Yin Mohd Khairul Nizam Mohd Khalid Ngu Lock Hock

Glutaric aciduria type 1 (GA1) is an autosomal recessive metabolic disorder caused by deficiency of glutaryl-CoA dehydrogenase enzyme encoded by the GCDH gene. In this study, we presented the clinical and molecular findings of seven GA1 patients in Malaysia. All the patients were symptomatic from infancy and diagnosed clinically from large excretion of glutaric and 3-hydroxyglutaric acids. Bidi...

Journal: :Archives of disease in childhood 1976
T C Stamp L R Baker

Two out of 3 children of a first-cousin marriage presented with severe rickets in infancy and are now adult. Their disease has shown continued activity, marked resistance to treatment with vitamin D, early fusion of cranial sutures, greatly increased bone density, nerve deafness, and life-long hypophosphataemia unaffected by treatment. Both parents and a third sib were normal clinically and bio...

Journal: :Sudanese journal of paediatrics 2015
Abdelakarim Ibrahim Abbaker Ali Saeed Dammas

Primary familial hemophagocytic lymphohistiocytosis (HLH; or familial erythrophagocytic lymphohistiocytosis [FEL]) is a heterogeneous autosomal recessive disorder more prevalent with parental consanguinity. There is aggressive proliferation of activated macrophages and histiocytes, which phagocytose red blood cells (RBCs), white blood cells (WBCs), and platelets, leading to anemia, neutropenia ...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1984
Y Mitsuyama

The clinico-pathological findings of 26 cases of presenile dementia with motor neuron disease in Japan are reviewed. The characteristic features include: (1) Progressive dementia with slowly progressive onset in the presenile period. (2) Neurogenic muscular wasting during the course of illness. (3) A duration of illness to death of from one to three years. (4) Absence of extrapyramidal symptoms...

Journal: :American journal of medical genetics. Part A 2009
Carmelo Damiano Salpietro Silvana Briuglia Maria Concetta Cutrupi Romina Gallizzi Luciana Rigoli Bruno Dallapiccola

Mastocytosis refers to a heterogeneous group of rare disorders characterized by an abnormal accumulation of mast cells in one or more organ systems. Cutaneous mastocytosis (CM) is the most frequent form in children and is characterized by hyperpigmented macules or papules symmetrically distributed over the trunk, and less so over the limbs, neck, and scalp. Two published articles have reported ...

Journal: :Journal of medical genetics 1980
I Tamari R M Goodman I Sarova M Hertz R Adar T Zvibach

Three unrelated Oriental Jewish families with a total of eight subjects with progressive hereditary sensory neuropathy are reported. The parents were all unaffected and because of parental consanguinity in each of the three families it is postulated that this rare neurological disorder is transmitted in an autosomal recessive manner. In one family both parents showed an abnormal response to pai...

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