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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] Beginning in childhood, those affected become constantly hungry, which often leads to obesity and type 2 diabetes. [2]

  3. Chromosome 15 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_15

    People normally have two copies of this chromosome in each cell, one copy from each parent. PraderWilli syndrome occurs when the paternal copy is partly or entirely missing. In about 70% of cases, [citation needed] PraderWilli syndrome occurs when the 15q11-q13 region of the paternal chromosome 15 is deleted. The genes in this region are ...

  4. 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.

  5. Heinrich Willi - Wikipedia

    en.wikipedia.org/wiki/Heinrich_Willi

    Heinrich Willi (4 March 1900 – 16 February 1971) was a Swiss pediatrician who specialised in neonatology and co-discovered PraderWilli syndrome with Andrea Prader. Biography [ edit ]

  6. List of congenital disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_congenital_disorders

    Sotos syndrome Cerebral Gigantism; ... PraderWilli syndrome; Proteus syndrome; Prune belly syndrome; R ... Statistics; Cookie statement;

  7. Urban–Rogers–Meyer syndrome - Wikipedia

    en.wikipedia.org/wiki/Urban–Rogers–Meyer...

    Urban–Rogers–Meyer syndrome, also known as PraderWilli habitus, osteopenia, and camptodactyly or Urban syndrome, [1] is an extremely rare inherited congenital disorder first described by Urban et al. (1979).

  8. What is Angelman Syndrome, the disease affecting Colin ...

    www.aol.com/angelman-syndrome-disease-affecting...

    "Angelman syndrome shares symptoms and characteristics with other disorders including autism, cerebral palsy and Prader-Willi syndrome," read the Angelman Syndrome Foundation website. "People with ...

  9. Genomic imprinting - Wikipedia

    en.wikipedia.org/wiki/Genomic_imprinting

    The first imprinted genetic disorders to be described in humans were the reciprocally inherited Prader-Willi syndrome and Angelman syndrome. Both syndromes are associated with loss of the chromosomal region 15q11-13 (band 11 of the long arm of chromosome 15).