Related Experiment Videos
A 68-year-old white female with Prader-Willi syndrome
Clinical Dysmorphology
|January 29, 2000
Abstract:
A 68-year-old white female with Prader-Willi syndrome is described. The clinical features are described and the progression of her condition is discussed and illustrated.
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder.
Journal of intellectual disability research : JIDR·2017
Examination of Global Methylation and Targeted Imprinted Genes in Prader-Willi Syndrome.
Journal of clinical epigenetics·2017
EVALUATION OF PLASMA SUBSTANCE P AND BETA-ENDORPHIN LEVELS IN CHILDREN WITH PRADER-WILLI SYNDROME.
The Journal of rare disorders·2016
Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
Journal of endocrinological investigation·2015
Monochorionic dizygotic twins with discordant genetic findings and congenital malformations.
Clinical dysmorphology·2026
Oculoskeletodental syndrome: expansion and review of the clinical and molecular phenotype.
Clinical dysmorphology·2026
Real-world treatment patterns and persistent symptoms in adults with depression undergoing antidepressant treatment.
Journal of affective disorders·2026
Patient-reported outcome measures for depression or anxiety symptoms in patients with cardiovascular disease: A COSMIN systematic review.
Journal of psychosomatic research·2026
Beyond the clinic: The role of the psychiatrist in practicing pragmatic solidarity.
PLOS mental health·2026
Development of Japanese Versions of the 4-Item Mystical Experience Questionnaire and 7-Item Challenging Experience Questionnaire.
Neuropsychopharmacology reports·2026