نتایج جستجو برای: autosomal recessive

تعداد نتایج: 41260  

Journal: :Journal of Mahatma Gandhi Institute of Medical Sciences 2016

Mansour Heidari

Amelogenesis Imperfectas (AIs) are clinically and genetically heterogeneous conditions characterized by a wide range of clinical features. These abnormalities of enamel formation are categorized into three main groups, hypoplastic, hypomaturation and hypocalcified with different modes of inheritance such as autosomal recessive (AR), autosomal dominant (AD) and X-lined recessive (XLR). In spite ...

صادقی, زهرا, فروغمند, علی محمد, محمدیان, غلامرضا,

Background and purpose: Microcephaly is reduced head circumference more than two standard deviation below the mean for the age and sex. Genetic microcephaly disorder is divided into two categories; isolated and syndromic microcephaly. The incidence of autosomal recessive primary microcephaly in consanguineous population is more than that in non-consanguineous population. So far, few studies are...

2016
Celeste Montecchiani Lucia Pedace Temistocle Lo Giudice Antonella Casella Marzia Mearini Fabrizio Gaudiello José L. Pedroso Chiara Terracciano Carlo Caltagirone Roberto Massa Peter H. St George-Hyslop Orlando G. P. Barsottini Toshitaka Kawarai Antonio Orlacchio

Charcot-Marie-Tooth disease is a group of hereditary peripheral neuropathies that share clinical characteristics of progressive distal muscle weakness and atrophy, foot deformities, distal sensory loss, as well as diminished tendon reflexes. Hundreds of causative DNA changes have been found, but much of the genetic basis of the disease is still unexplained. Mutations in the ALS5/SPG11/KIAA1840 ...

Journal: :Journal of medical genetics 1984
A Richieri-Costa S M Garcia da Silva O Frota-Pessoa

Four sibs of non-consanguineous parents who had myotonia from late infancy are described. Mild to moderate mental retardation, severe bone abnormalities of the vertebral column (mainly in the thoracolumbar region), and short stature were also observed. Autosomal recessive inheritance is demonstrated. These cases are compared with reported cases of the Schwartz-Jampel syndrome.

2017
Mariam S Al Harbi Ayman W El-Hattab

Protein C is an anticoagulant that is encoded by the PROC gene. Protein C deficiency (PCD) is inherited in an autosomal dominant or recessive pattern. Autosomal dominant PCD is caused by monoallelic mutations in PROC and often presents with venous thromboembolism. On the other hand, biallelic PROC mutations lead to autosomal recessive PCD which is a more severe disease that typically presents i...

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