From the clinical to the genetic diagnosis of Prader-Willi and Angelman syndromes

Keyphrases

• Genetic Diagnosis 100%
• Prader-Willi Syndrome 100%
• Angelman Syndrome 100%
• Intellectual Disability 66%
• Genetic Mechanism 66%
• Genetic Counseling 33%
• Obesity 33%
• Behavioral Phenotype 33%
• Hypogonadism 33%
• Ataxia 33%
• Clinical Diagnosis 33%
• Hyperactivity 33%
• Microcephaly 33%
• Chromosome 15 33%
• Diagnostic Algorithm 33%
• Tremor 33%
• Behavioral Disorders 33%
• Genomic Imprinting 33%
• Hypotonia 33%
• 15q11-q13 33%
• Feeding Difficulties 33%
• Neonatal Period 33%
• Convulsion 33%
• UBE3A 33%

Biochemistry, Genetics and Molecular Biology

• Prader-Willi Syndrome 100%
• Genetics 100%
• Angelman Syndrome 100%
• Genetic Mechanism 66%
• Genomic Imprinting 33%
• Genetic Counseling 33%
• UBE3A 33%
• Cognition 33%
• Chromosome 15 33%
• Newborn Period 33%

Neuroscience

• Angelman Syndrome 100%
• Prader Willi Syndrome 100%
• Microcephaly 33%
• Hypotonia 33%
• Behavior (Neuroscience) 33%
• Tremor 33%
• Ataxia 33%
• Hypogonadism 33%
• Hyperactivity 33%
• Chromosome 15 33%
• Behavior Disorder 33%