Pallister Killian Mosaic Syndrome Genetic Disorders Conditions and Diseases

Pallister Killian Mosaic Syndrome Genetic Disorders Conditions and Diseases

Pallister-Killian Mosaic Syndrome is a rare chromosomal disorder that occurs for no apparent reason. Major symptoms may include a coarse face with a high forehead, sparse hair on the scalp, an abnormally wide space between the eyes, a fold of the skin over the inner corner of the eyes, and a broad nasal bridge with a highly arched palate. Mental retardation, loss of muscle tone, and streaks of skin lacking color are often present.

Top: Health: Conditions and Diseases: Genetic Disorders: Pallister Killian Mosaic Syndrome

Editor's Picks:

PKS Kids

- Includes biographies and photos of children with the syndrome, first-hand information from parents, and links to related support and equipment resources.

OrphaNet: Tetrasomy 12p - A collection of global organizations and support groups related to the genetic condition.
NORD: Pallister Killian Mosaic Syndrome - Offers the synonyms, a general discussion and further resources.
PKS Support - An online support group, with a discussion forum, family photos and informal surveys.
Pallister-Killian Mosaic Syndrome - Offers overview, support and news in English and Italian.
National Library of Medicine - The synonyms of chromosome 12p tetrasomy syndrome, a summary and a list of major features.
Frappr Maps: PKS Support - A map of individuals with the condition around the world, including photos.
Bigger than our Bodies - Contains news, events and links related to PKS.
Jake's World - Features the biography, photos and videos of a child with PKS.

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