Conditions And Diseases - Pallister Killian Mosaic Syndrome Top Links Healthcare Industry, Medicine, Men's Health. pallister killian mosaic syndrome Web Site Links. NORD pallister killian mosaic syndrome - Offers the synonyms, a general discussion and http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso
Pallister-Killian Syndrome PallisterKillian Syndrome resources, links to national and international support groups, clinics with genetic counselors and geneticists Pallister-Killian syndrome. Pallister-Killian Syndrome Family Support Group or birth defects. pallister killian mosaic syndrome, National Organization for Rare Disorders. Pallister http://www.kumc.edu/gec/support/palliste.html
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Pallister Killian Mosaic Syndrome - Quest Diagnostics Patient Health Library PallisterKillian Mosaic Syndrome is a rare chromosomal disorder caused by the presence of four copies of the short arm of chromosome 12 instead of the normal two. Major symptoms may include a pallister killian mosaic syndrome. Important. It is possible that the main title of the report is not http://www.questdiagnostics.com/kbase/nord/nord512.htm
Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Pallister-Killian Mosaic Syndrome is a rare chromosomal disorder caused by the presence of four copies of the short arm of chromosome 12 instead of the normal two. 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. The Arc (a national organization on mental retardation)
Pallister Killian Mosaic Syndrome PallisterKillian Mosaic Syndrome is a rare chromosomal disorder caused by the presence of four copies of the short arm of chromosome 12 instead of the normal http://www.bchealthguide.org/kbase/nord/nord512.htm
Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Information on the following diseases can be found in the Related Disorders section of this report: Pallister-Killian Mosaic Syndrome is a rare chromosomal disorder caused by the presence of four copies of the short arm of chromosome 12 instead of the normal two. 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. Individuals with Pallister-Killian Mosaic Syndrome typically have low muscle tone at birth (hypotonia), sparse scalp hair, a high forehead, a coarse face, an abnormally wide space between the eyes, a broad nasal bridge, a highly arched palate, a fold of the skin over the inner corner of the eyes, and large ears with lobes that are thick and protrude outward.
Fryns Syndrome Trisomy 18 syndrome; pallister killian mosaic syndrome; Cornelia de Lange syndrome. PallisterKillian mosaic syndrome is caused by tetrasomy for chromosome 12p. http://www.bchealthguide.org/kbase/nord/nord959.htm
Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Information on the following diseases can be found in the Related Disorders section of this report: Fryns syndrome is an extremely rare inherited disorder characterized by multiple abnormalities that are present at birth (congenital). Characteristic symptoms and physical findings include protrusion of part of the stomach and/or small intestines into the chest cavity (diaphragmatic hernia), abnormalities of the head and face area (craniofacial region), and underdevelopment of the ends of the fingers and toes (distal digit hypoplasia). Additional symptoms include underdevelopment (hypoplasia) of the lungs, incomplete closure of the roof of the mouth (cleft palate), cardiac defects, and varying degrees of mental retardation. Fryns syndrome is inherited as an autosomal recessive trait. Fryns syndrome is associated with numerous abnormalities of varying severity such as protrusion of part of the stomach and/or small intestines into the chest cavity (diaphragmatic hernia), unusual facial features, and abnormalities of the fingers and toes. The number and severity of symptoms and physical findings will vary greatly from case to case.
Pallister Killian Mosaic Syndrome pallister killian mosaic syndrome Important It is possible that the main title of the report pallister killian mosaic syndrome is not the name you expected. http://my.webmd.com/hw/raising_a_family/nord512.asp
Extractions: Pallister-Killian Mosaic Syndrome is a rare chromosomal disorder caused by the presence of four copies of the short arm of chromosome 12 instead of the normal two. 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.
Pallister Killian Mosaic Syndrome @ Www.Sweden.org Home pallister killian mosaic syndrome (3), Website related to pallister killian mosaic syndrome National Library of Medicine The http://www.sweden.org/Health/Conditions_and_Diseases/Genetic_Disorders/Pallister
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Extractions: Ablepharon-Macrostomia Syndrome ... Genetic Disorders : Pallister Killian Mosaic Syndrome National Library of Medicine - The synonyms of Killian syndrome, a summary and a list of major features. NORD: Popliteal Pterygium Syndrome - Offers synonyms, a general discussion and further resources. Pediatric Database - A definition of Pallister-Killian syndrome, the epidemiology, pathogenesis, clinical features, investigations and management.
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Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Pallister Killian Mosaic Syndrome Web Sites National Library of Medicine [Site Info] [Translate] [Open New Window] NORD: Pallister Killian Mosaic Syndrome [Site Info] [Translate] [Open New Window] Offers the synonyms, a general discussion and further resources. URL: http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Pallister%20Killian%20Mosaic%20Syndrome
Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Rare Disorders Web Sites National Organization for Rare Disorders, Inc. [Site Info] [Translate] [Open New Window] Information about NORD, its programs, special events and the variety of services offered. Includes a rare disease, organization and orphan drug database. Diseases are listed alphabetically for easy searching. URL: http://www.rarediseases.org/
Genetic Disorders: Pallister Killian Mosaic Syndrome Genetic Disorders pallister killian mosaic syndrome. Home Health Conditions and Diseases Genetic Disorders pallister killian mosaic syndrome. http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/Pa
