Diagnosis of Prader-Willi Syndrome and Angelman Syndrome
NCT04155944 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60
Last updated 2023-04-07
Summary
In a retrospective study, data were assessed from cases regarding PWS/AS that underwent molecular diagnosis at the National Chen-Kung University Hospital, Tainan, Taiwan, between January 2001 and December 2014.
Conditions
- Mental Disorder
- Fetus Disorder
Sponsors & Collaborators
-
National Cheng-Kung University Hospital
lead OTHER
Principal Investigators
-
Pao-Lin Kuo, MD · Department of Obstetrics and Gynecology, National Chen-Kung University Hospital
Eligibility
- Max Age
- 45 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-08-31
- Primary Completion
- 2014-12-31
- Completion
- 2014-12-31
Countries
- Taiwan
Study Locations
More Related Trials
-
Evaluation of Placenta Maturity by the Sonographic Textures
NCT01255930 ·Status: UNKNOWN
-
Use Cord Blood Single Nucleotide Polymorphism to Predict the Later Development of Atopy and Allergy
NCT00444327 ·Status: UNKNOWN
-
Verification of the Epidemiology and Mortality of Rare Diseases in Taiwan With Real-world Evidence
NCT05367115 ·Status: COMPLETED
-
Mutation Analysis of 17βhydroxysteroid Dehydrogenase 3 Deficiency
NCT00173654 ·Status: UNKNOWN
-
Clinical Outcome of Pediatric Dermatofibrosarcoma Protuberans
NCT00173355 ·Status: UNKNOWN
-
The Factors That Affected the Outcome of Treatment of Congenital Nasolacrimal Duct Obstruction
NCT02081781 ·Status: COMPLETED
-
A Long-term Study for the Outcome of Pompe Disease
NCT02399748 ·Status: RECRUITING
-
Chinese AntiphosPholipid Syndrome cohorT cOllaborative NEtworks
NCT05230017 ·Status: RECRUITING
-
A Long Term Follow up Study in Late-onset Pompe Disease
NCT00713245 ·Status: UNKNOWN
-
Genetic Polymorphism and Retinopathy of Prematurity: Correlation of Clinical Presentations and Severity
NCT05132257 ·Status: UNKNOWN
-
Muscle Response to Enzyme Replacement Therapy in Pompe Disease
NCT00713453 ·Status: UNKNOWN
-
Investigation of Human Alpha-fetoprotein Genes
NCT01258894 ·Status: UNKNOWN
-
the Correlation Between Non-invasive Indicators in Patients With Biliary Atresia
NCT02848573 ·Status: COMPLETED
-
Angiotensin Converting Enzyme Gene Polymorphism in Children With Idiopathic Nephrotic Syndrome
NCT00172276 ·Status: COMPLETED
-
Genetic Biomarkers Associated With Child Language Development in Taiwan (II)
NCT05510570 ·Status: COMPLETED
-
The Genetic Study of Primary Angle-Closure Glaucoma
NCT00155857 ·Status: UNKNOWN
-
A Retrospective Study for Multiple Endocrine Neoplasia
NCT05812573 ·Status: UNKNOWN
-
Catecholamines Can Attenuate Intermittent Hypoxia-Induced Expression of TNF in Human Monocytes
NCT00498862 ·Status: UNKNOWN
-
Child Development and Genetic Biomarkers
NCT04660942 ·Status: UNKNOWN
-
Application of Genetic Polymorphisms of DNA Repair in The Prediction of Prostate Cancer Susceptibility and Its Clinical Outcome
NCT00167024 ·Status: UNKNOWN
-
Exploring the Possibility to Use Glycosyltransferase as a Prognosis Marker of Neuroblastoma
NCT01638572 ·Status: COMPLETED
-
Studies of Biomarkers in Female Lower Urinary Tract Symptoms
NCT01681784 ·Status: UNKNOWN
-
Newborn Screening for Adrenoleukodystrophy
NCT02952482 ·Status: COMPLETED
-
Genetic Biomarkers of Child Language Development in Taiwan: an Identification and Validation Study
NCT05504564 ·Status: UNKNOWN
-
Genetic Biomarkers Associated With Child Language Development in Taiwan
NCT04518787 ·Status: UNKNOWN