"Never mind, when is dinner ready?" Living with Prader-Willi syndrome

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"Never mind, when is dinner ready?" Living with Prader-Willi syndrome.

''Never mind, when is dinner ready?'' Living with Prader-Willi syndrome T he cat died when Rachel was 15J. Ginger was loved and cuddled by Rachel every day for every one of his 12 years. Ginger's life was defined by the search for warmth on Rachel's bed and a regular supply of food. Rachel's chromosomes determine that her life is lived through the experience of Prader-Willi syndrome. It is unfo...

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Dental Management of Patients with Prader Willi Syndrome

Prader–Willi syndrome (PWS) is a genetic disorder which occurs with a frequency of about one in 10,000–30,000 live newborns. Both males and females, and all races are equally affected. PWS is a complex disorder with multiple disabilities, and the main defect is found in the hypothalamus. Child with PWS at the age between 2 and 3 years becomes constantly hungry and if the diet is not controlled,...

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Prader-Willi Syndrome

Prader-Willi syndrome is a neurogenetic disorder characterized by hypotonia and feeding difficulties in infancy, followed by hyperphagia, hypogonadism, mental retardation, and short stature. It was the first recognized microdeletion syndrome identified with high-resolution chromosome analysis, the first recognized human genomic imprinting disorder, and the first recognized disorder resulting fr...

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Prader-Willi syndrome.

Prader-Willi syndrome is a multi system disorder characterized by neonatal hypotonia, later obesity, hyperphagia and mental retardation. It occurs sporadically, either as a result of microdeletion of chromosome 15p (70%) or as a result of maternal disomy of chromosome 15 (30%). The major problems encountered by parents are those of hyperphagia, food-seeking and obesity, and conduct disorder, pa...

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Prader-willi Syndrome

Prader–Willi syndrome (PWS) is a genetic disorder due to loss of function of specific genes on chromosome 15. It occurs in males and females, no matter what race. As an infant, PWS shows itself in weak muscle tone (hypotonia, Pic. 1), feeding difficulties, poor growth, and delayed development. In the beginning during childhood, characterizes itself by having the kids develop an insatiable appet...

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood

سال: 2005

ISSN: 0003-9888,1468-2044

DOI: 10.1136/adc.2004.050021