Literature DB >> 3688026

Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion.

S L Wenger1, J M Hanchett, M W Steele, B V Maier, W L Golden.   

Abstract

Fifty-nine patients with Prader-Willi syndrome (PWS) (including three blacks) were enrolled in a behavior modification program including dietary restriction, nutritional education for self-management of food intake, and exercise. Caloric intake for most patients was 700-800 calories per day. The average stay per patient was 5 weeks with a mean weight loss of 6.6 kg. Thirty-one patients (53%) had apparently normal chromosomes compared to 25 patients (42%) with apparent 15(q12) deletion. Three patients had other chromosome abnormalities including two with mosaicism for idic(15)(q11) and one with a de novo apparently balanced translocation t(8q;18q). There were no differences in manifestations or the effects of the behavior modification program between chromosomally normal and abnormal patients. However, the mean weight loss in the 59 PWS patients was less than would have been expected based on their calculated daily caloric requirements suggesting that PWS patients have reduced caloric needs per unit of body weight compared to normal individuals. Supporting this also was that weight maintenance could be accomplished with only 1000 calories per day on the average. In general, behavioral response to the modification program was successful in that tantrum responses, while not eliminated, were reduced in frequency and severity.

Entities:  

Mesh:

Year:  1987        PMID: 3688026     DOI: 10.1002/ajmg.1320280413

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

1.  Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype.

Authors:  C E Wallis; P H Beighton
Journal:  J Med Genet       Date:  1989-05       Impact factor: 6.318

2.  INTRAFAMILIAL AND MIDPARENTAL-CHILD CORRELATIONS AND HERITABILITY ESTIMATES OF ANTHROPOMETRIC MEASUREMENTS IN PRADER-WILLI SYNDROME FAMILIES.

Authors:  Merlin G Butler; Judy L Haynes; F John Meaney
Journal:  Dysmorphol Clin Genet       Date:  1990

3.  Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome.

Authors:  G Gillessen-Kaesbach; W Robinson; D Lohmann; S Kaya-Westerloh; E Passarge; B Horsthemke
Journal:  Hum Genet       Date:  1995-12       Impact factor: 4.132

4.  A genetic model for the Prader-Willi syndrome and its implication for Angelman syndrome.

Authors:  I Kennerknecht
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

5.  Sister chromatid exchange analysis of the 15q11 region in Prader-Willi syndrome patients.

Authors:  S L Wenger; S D Rauch; J M Hanchett
Journal:  Hum Genet       Date:  1989-09       Impact factor: 4.132

6.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03

7.  Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.

Authors:  M G Butler
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025

8.  Anthropometric study with emphasis on hand and foot measurements in the Prader-Willi syndrome: sex, age and chromosome effects.

Authors:  M G Butler; J L Haynes; F J Meaney
Journal:  Clin Genet       Date:  1991-01       Impact factor: 4.438

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.