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Prader-Willi psychiatric syndrome and Velo-Cardio-Facial psychiatric syndrome

Autor: W M, Verhoeven, S, Tuinier, L M, Curfs

Publikováno v: Genetic counseling (Geneva, Switzerland). 11(3)

Prader-Willi psychiatric syndrome and Velo-Cardio-Facial psychiatric syndrome: Similar to the studies on behavioural phenotypes, it is suggested to more rigorously promote the investigation of psychopathological phenotypes. The psychopathological pro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::731c957ee73f1f0f9c7948f910140b04
https://pubmed.ncbi.nlm.nih.gov/11043428

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Management of sleeping problems in Wolf-Hirschhorn syndrome: a case study

Autor: L M, Curfs, R, Didden, S P, Sikkema, C E, De Die-Smulders

Publikováno v: Genetic counseling (Geneva, Switzerland). 10(4)

Sleeping problems are common among children with Wolf-Hirschhorn syndrome. Extinction may be effective if sleeping problems have been shaped and are positively reinforced by parental attention. The present study shows that extinction was effective in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::049b27556f5363262c7d49c805e2a252
https://pubmed.ncbi.nlm.nih.gov/10631921

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Prader-Willi syndrome and psychotic symptoms: 1. Case descriptions and genetic studies

Autor: D, Clarke, H, Boer, T, Webb, P, Scott, S, Frazer, A, Vogels, M, Borghgraef, L M, Curfs

Publikováno v: Journal of intellectual disability research : JIDR. 42

Six people with Prader-Willi syndrome (PWS) who developed psychoses are described. Along with other literature reviewed in the present paper, the results imply an association between PWS and psychotic symptoms. Genetic studies were possible in five c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b812bc720850ccc5f917bc0bc9c35e39
https://pubmed.ncbi.nlm.nih.gov/10030439

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Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome

Autor: C F, van Lieshout, R E, De Meyer, L M, Curfs, J P, Fryns

Publikováno v: Journal of child psychology and psychiatry, and allied disciplines. 39(5)

The personality profiles for youths with Prader-Willi, fragile-X, or Williams syndrome were compared to three matched groups attending regular schools. Using the California Child Q-Set (CCQ), both of the parents of the 39 children with Prader-Willi s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2b3fd6bf9e9a7d2e997cbfce6ea4ccd6
https://pubmed.ncbi.nlm.nih.gov/9690933

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Functional assessment and treatment of sleeping problems with developmentally disabled children: six case studies

Autor: R, Didden, L M, Curfs, S P, Sikkema, J, de Moor

Publikováno v: Journal of behavior therapy and experimental psychiatry. 29(1)

Sleeping problems are common among developmentally disabled children of young age and they may have adverse effects on the well-being of both child and parents. In the present study, results from functional assessment with four children suggested tha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bb25f40900d41350f01f4e91bd036540
https://pubmed.ncbi.nlm.nih.gov/9627828

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Hyperacusis in Williams syndrome: a sample survey study

Autor: J, Van Borsel, L M, Curfs, J P, Fryns

Publikováno v: Genetic counseling (Geneva, Switzerland). 8(2)

Williams syndrome is a true multiple congenital anomalies mental retardation syndrome affecting the vascular, connective tissue and the central nervous system. Affected individuals have a distinctive neuropsychological profile characterized by extrem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cde6773aff8cd58bb7e36094547eab0c
https://pubmed.ncbi.nlm.nih.gov/9219010

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The Prader-Willi syndrome: a self supporting program for children, youngsters and adults

Autor: M J, Descheemaeker, A, Swillen, L, Plissart, M, Borghgraef, S, Rasenberg, L M, Curfs, J P, Fryns

Publikováno v: Genetic counseling (Geneva, Switzerland). 5(2)

The Prader-Willi syndrome is characterized by four cardinal symptoms i.e. hypotonia, hypogonadism, mental retardation and extreme obesity. Behavioural and psychological problems are frequent in these patients, mostly related to the withholding of foo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::df18619b769f0b2b766c8c03ce18bb25
https://pubmed.ncbi.nlm.nih.gov/7917134

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A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features

Autor: A M, Wiegers, L M, Curfs, H, Meijer, B, Oostra, J P, Fryns

Publikováno v: Genetic counseling (Geneva, Switzerland). 5(4)

In this report we present the results of psychological investigations in a family in which 11 individuals, 7 females and 4 males, have a deletion of 1.6 Kb proximal to the CGG repeat of the FMR1. All 4 males with the deletion and 2 of the female carr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c3e36b874950f136e5926cc98b7c7a50
https://pubmed.ncbi.nlm.nih.gov/7888141

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