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Title: [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome]. Author: Witkowski R, Ullrich E, Pietsch P, Weber K, Heller K, Losanowa T, Nitz I. Journal: Psychiatr Neurol Med Psychol (Leipz); 1985 May; 37(5):255-61. PubMed ID: 4023109. Abstract: We present four cases of Prader-Willi syndrome. Two of them have an abnormality of a chromosome 15, the other both show different chromosomal abnormalities. Translocations or deletions were found recently in the bands 15q11/12 in about 60% of the cases of Prader-Willi syndrome. The consequences for diagnosis, symptomatology and genetic counselling of the syndrome are discussed.[Abstract] [Full Text] [Related] [New Search]