منابع مشابه
Deaf-Mutism
The author of this book pleads for indulgence to any shortcomings of language, on the ground that he is not an Englishman, but such indulgence is by no means necessary inasmuch as the language would do credit to any English writer. The book bristles with statistics which are, of course, drawn largely from Danish sources, but tables are also given from all countries ?f Europe as well as from Ame...
متن کاملPrevalence and genetic aspects of deaf mutism in Shanghai.
Two hundred and eighty-five cases of congenital deaf mutism were ascertained in a population of 483,611 in Zhabei District in Shanghai. The prevalence was 0.059% (1:1697). Inherited cases accounted for 84.83% of all cases. The mode of inheritance was autosomal recessive with complete penetrance and heterogeneity (consisting of at least five different loci). The fitness was 77.63%, the coefficie...
متن کاملConsanguinity, caste and deaf-mutism in Punjab, 1921.
The effects of religion, population sub-division and geography on the prevalence of deaf-mutism were investigated using information collected in the 1921 Census of Punjab. The total sample size was 9.36 million, and comprised data on thirteen Hindu castes, seventeen Muslim biraderis and two Sikh castes. A two-way analysis of variance comparing males in Hindu castes in which consanguineous marri...
متن کاملAbsence of Nails, Deaf-mutism, Seizures, and Intellectual Disability: A Case Report.
Seizures coexists in children with intellectual disability and are often attributed to neural dysfunction associated with it. Often a careful clinical examination will unravel many diagnostic pointers as in this 8-year-old child with global development delay, deaf-mutism and moderate intellectual disability (mental retardation) who presented with seizures in the emergency department. General ex...
متن کاملBrugada syndrome and calcium channel mutation in a patient with congenital deaf mutism
To the best of our knowledge, for the first time in the literature, we described a congenitally deaf-mute patient with Brugada syndrome (BrS) in whom a mutation in L-type Ca+2 channel [CACNA1C (Cav1.2α1)] was identified.
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ژورنال
عنوان ژورنال: The Lancet
سال: 1896
ISSN: 0140-6736
DOI: 10.1016/s0140-6736(01)74403-0