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  2. Prader–Willi syndrome - Wikipedia

    en.wikipedia.org/wiki/PraderWilli_syndrome

    PraderWilli syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. [2] In newborns , symptoms include weak muscles , poor feeding, and slow development. [ 2 ]

  3. Chromosomal deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_deletion_syndrome

    PraderWilli (PWS) and Angelman syndrome (AS) are distinct neurogenetic disorders caused by chromosomal deletions, uniparental disomy or loss of the imprinted gene expression in the 15q11-q13 region. Whether an individual exhibits PWS or AS depends on if there is a lack of the paternally expressed gene to contribute to the region. [citation ...

  4. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    D – Deletion of a gene or genes; Dup - Duplication of a gene or genes; C – Whole chromosome extra, missing, or both (see chromosome abnormality) T – Trinucleotide repeat disorders: gene is extended in length; Craniosynostosis can be found in several disorders, like Carpenter Syndrome

  5. What is Prader-Willi syndrome? [Video] - AOL

    www.aol.com/news/girl-chronic-overeating...

    A 15-year-old girl with a rare genetic condition that causes insatiable hunger just won a beauty pageant. Here's what you need to know about Prader-Willi Syndrome.

  6. 1p36 deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/1p36_deletion_syndrome

    1p36 deletion syndrome is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features. The symptoms may vary, depending on the exact location of the chromosomal deletion.

  7. Chromosome 15q partial deletion - Wikipedia

    en.wikipedia.org/wiki/Chromosome_15q_partial...

    The sister syndrome Prader-Willi syndrome (PWS) can result if the father's copy of the chromosomal region 15q11-13 is deleted. [2] The smallest observed region that can result in these syndromes when deleted is therefore called the PWS/AS critical region.

  8. NNZ-2591 - Wikipedia

    en.wikipedia.org/wiki/NNZ-2591

    NNZ-2591 is a synthetic analog of cyclic glycine-proline and experimental drug developed for Angelman syndrome, Phelan-McDermid syndrome, Pitt Hopkins syndrome, [1] [2] and Prader-Willi syndrome. [ 3 ]

  9. Woman Who Underwent Groundbreaking Cancer Treatment Has Been ...

    www.aol.com/woman-underwent-groundbreaking...

    The woman is likely “the longest-surviving patient with cancer who received CAR-T therapy,” the paper notes. “Encouragingly, she has subsequently had two full-term pregnancies with normal ...