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  2. 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).

  3. 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]

  4. Chromosomal deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_deletion_syndrome

    There are known three molecular causes of PraderWilli syndrome development. One of them consists in micro-deletions of the chromosome region 15q11–q13. 70% of patients present a 5–7-Mb de novo deletion in the proximal region of the paternal chromosome 15. The second frequent genetic abnormality (~ 25–30% of cases) is maternal ...

  5. 7-Day No-Sugar Meal Plan for Metabolic Syndrome, Created by a ...

    www.aol.com/7-day-no-sugar-meal-170000099.html

    Follow this 7-day no-sugar-added meal plan for a week of delicious recipes tailored to improve the conditions that make up metabolic syndrome. Photo: Will Dickey/Robby Lozano

  6. 7-Day Mediterranean Diet Meal Plan for Longevity, Created by ...

    www.aol.com/7-day-mediterranean-diet-meal...

    This 1,800-calorie meal plan has modifications for 1,500 and 2,000 calories to support those with different calorie needs. While we previously included meal plans and modifications for 1,200 ...

  7. Microdeletion syndrome - Wikipedia

    en.wikipedia.org/wiki/Microdeletion_syndrome

    DiGeorge syndrome or velocardiofacial syndrome [3] – most common microdeletion syndrome; PraderWilli syndrome [4] [5] Angelman syndrome [4] Neurofibromatosis type I [6] Neurofibromatosis type II [7] [8] Williams syndrome [9] Miller–Dieker syndrome [10] Smith–Magenis syndrome [11] Rubinstein–Taybi syndrome [12] Wolf–Hirschhorn ...

  8. Childhood obesity - Wikipedia

    en.wikipedia.org/wiki/Childhood_obesity

    PraderWilli syndrome, with an incidence between 1 in 12,000 and 1 in 15,000 live births, is characterized by hyperphagia and food preoccupations which leads to rapid weight gain in those affected. Bardet–Biedl syndrome; MOMO syndrome; Leptin receptor mutations; Congenital leptin deficiency; Melanocortin receptor mutations

  9. Obesity - Wikipedia

    en.wikipedia.org/wiki/Obesity

    Obesity is a major feature in several syndromes, such as PraderWilli syndrome, Bardet–Biedl syndrome, Cohen syndrome, and MOMO syndrome. (The term "non-syndromic obesity" is sometimes used to exclude these conditions.) [ 142 ] In people with early-onset severe obesity (defined by an onset before 10 years of age and body mass index over ...