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         Teschler-nicola Syndrome:     more detail

81. Open Classes's $p->page_title
Svenska Open Directory Health Conditions and Diseases GeneticDisorders Pallister Killian Mosaic syndrome Previous Catagory.
http://dodo101.ath.cx/expat/odp.php/Health/Conditions_and_Diseases/Genetic_Disor
Open Directory Edit Add URL Update URL Description ... Svenska Open Directory - Health: Conditions and Diseases: Genetic Disorders: Pallister Killian Mosaic Syndrome [ Previous Catagory See also: Open Directory - Health: Conditions and Diseases: Genetic Disorders: Pallister Killian Mosaic Syndrome [ Previous Catagory All the Web AltaVista Deja Google ... Yahoo Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor

82. Pallister Killian Mosaic Syndrome Websites From Linkspider.org
Directory Results for Pallister Killian Mosaic syndrome from Linkspider.org.Keyword Pallister Killian Mosaic syndrome. Linkspider
http://www.linkspider.org/Health/ConditionsandDiseases/GeneticDisorders/Palliste
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83. Pallister Killian Mosaic Syndrome Website(s)
Directory Results for Pallister Killian Mosaic syndrome. Online KeywordPallister Killian Mosaic syndrome. Whizseek Directory Pallister
http://www.whizseek.com/Health/ConditionsandDiseases/GeneticDisorders/PallisterK
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84. ORPHANET® : Base De Données Sur Les Maladies Rares Et Les Médicaments Orpheli
Isochromosome 12p en mosaïque. Critères de diagnostic/définition.
http://orphanet.infobiogen.fr/data/patho/FR/fr-12p.html
Auteur: Docteur Nicole Morichon-Delvallez
Editeur scientifique: Professeur Didier Lacombe
Nom de la maladie et de ses synonymes

Incidence

Description clinique

Mode de prise en charge
...
Etiologie
Nom de la maladie et de ses synonymes
  • Syndrome de Pallister-Killian Syndrome de Pallister-Killian-Teschler-Nicola Syndrome de Teschler-Nicola-Killian
Incidence
Description clinique
Mode de prise en charge
Etiologie
in vitro avec l'augmentation du nombre des divisions cellulaires.
de novo
Cormier-Daire V, Le Merrer M, Gigarel N, Morichon N, Prieur M, Lyonnet S, Vekemans M, Munnich A. Prezygotic origin of the isochromosome 12pin Pallister-Killian syndrome. Am. J. Med. Genet. 1997 ; 69 : 166-168. Hunter AGW, Clifford B, M. Cox D. The characteristic physiognomy and tissue specific karyotype distribution in the Pallister-Killian syndrome. Clin. Genet. 1985 ; 28 : 47-53. Mauceri, L.; Sorge, G.; Incorpora, G.; Pavone, L. Pallister-Killian syndrome: case report with pineal tumor. Am. J. Med. Genet. 95: 75-78, 2000. Paladini D, Borghese A, Arienzo M, Teodoro A, Martinelli P, Nappi C. Prospective ultrasound diagnosis of Pallister-Killian syndrome in the second trimester of pregnancy: the importance of the fetal facial profile. Prenat Diagn. 2000 ; 20 : 996-8.

85. Malattie Rare E Genetiche Lettera "K"
Enfermedad deKikuchi Fujimoto Enfermedad de•{} * Killian Sindrome di•Killiansyndrome••Killian, Síndrome de Teschler Nicola Killian, Síndrome de
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KABUKI SINDROME DELLA MASCHERA
Sindrome della maschera di Kabuki Kabuki make-up, sindrome

86. T Information Sites
HEALTHorgs.com. Search The Largest Human Reviewed Health Databaseon Internet (Not sure of spelling? Use first letters and * such
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87. Our Services - Geisinger Health System Dermatology
Arch Dermatol 2000;1361263. Ohman A, Pride HB, Papa CA. Killian/TeschlerNicolasyndrome. Pediatr Dermatol 2000;17151-153. Acropustulosis
http://www.geisinger.org/services/dermatology/pride_pub.shtml
Publications
Howard Pride, M.D. Francis E, Pride HB, Tyler WB. A 16-year-old girl with epidermolysis bullosa acquisita (in preparation) Edwards K, Pride HB, Tyler WB. Indeterminate Cell Histiocytosis (in preparation) Jewel M, Pride HB. Congenital erythropoietic porphyria with extensive blister after phototherapy (in preparation) Suranyi E, Pride HB, Tyler WB. Hypohidrotic ectodermal dysplasia presenting as a collodion baby. J Am Acad Dermatol. (accepted and awaiting publication) Pelle M, Pride HB, Tyler WB. Eccrine angiomatous hamartoma: A report of four cases and review of the literature. J Am Acad Dermatol 2002;47:

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    unterstrichen, books underlined) 1. (1969) Snakebite by Aspidomorphus muelleri. The Medical Journal of Australia 1,10: 516-517 2. (1969) Student in Papua. med ass 1,1: 37 3. (1969) Medizinmann - Magier und Arzt. med ass 1,2: 20-24 6. (1971) Von Geistern und Menschen, med ass 3: 9/10: 28-32 und 28-30 (ebenfalls abgedruckt in: Der Medizinstudent 6: 9-10) 8. (1971) Aspects of the Medical System of the Kaluli and Waragu Language-Group, Southern Highlands District. Mankind 8: 141-145 9. (1974) Is the Role of the Sorcerer in Melanesian Medicine Outdated? Proceedings of the XXIII International Congress of the History of Medicine,London 2-9 Sept. 1972. Wellcome Institute of the History of Medicine. 2:1243-1247 Homo 26,4: 263-275 Kurth, Barmstedt. 14. (1977) "JAMU" - Traditionelle Medizin in Indonesien. Mitteilungen der Arbeitsgemeinschaft Ethnomedizin:5 u. 9. 15. (1977) Anmerkungen zum Film "Paranormale Heilmethoden auf den Philippinen" von Prof. Schiebeler. Beilage zum Filmbegleitheft des Instituts für den wissenschaftlichenFilm. Göttingen.

90. ÊÀÐÄÈÎËÎÃÈß ÄÅÒÑÊÎÃÎ ÂÎÇÐÀÑÒÀ
The summary for this Russian page contains characters that cannot be correctly displayed in this language/character set.
http://www.mks.ru/library/books/bum/kniga04/article02.html
1q32qter Trisomy
1q23 èëè 5qter Trisomy
Ôåíîòèï. Òîò æå, ÷òî è ïðè 1q32 qter, îäíàêî âèñöåðàëüíûå àíîìàëèè áîëåå âûðàæåíû.
1p25 q32 Trisomy
dup(1p3135)
Êàðèîòèï 46,XY,dir dup(pter31::p35p31::p31qter)
1q4 Monosomy
1q34-43 duplicated 1q44 deleted
2p2 Trisomy
2q3 Trisomy
Ôåíîòèï. Ìèêðîöåôàëèÿ, ìèêðîãíàòèÿ, ãèïåðòåëîðèçì, êîðîòêèé íîñ, òîíêèå ðóêè,"âûâåðíóòûå" íîãè, êèôîñêîëèîç, âîðîíêîîáðàçíàÿ äåôîðìàöèÿ ãðóäíîé êëåòêè, óìñòâåííàÿ îòñòàëîñòü (IQ îêîëî 50).
3p2 Trisomy
3p (p21 leads to 3pter) [karyotype: 46,XX,-6,+t(3;6)(6pter leads to 6q27::3p21 leads to 3pter)]
3q2 Trisomy
4p Trisomy
4q2 è 3 Trisomy Ôåíîòèï. Ìèêðîöåôàëèÿ, áðàõèöåôàëèÿ, äëèííûé íîñ, êîðîòêèå ðóêè, àíîìàëèè ãåíèòàëèé, êðèïòîðõèçì, àíîìàëèè ïî÷åê (ãèïîïëàçèÿ, ãèäðîíåôðîç), óìñòâåííàÿ îòñòàëîñòü (IQ=50).
4p Monosomy (ñèíäðîì Âîëüôà)
4q3 Monosomy
4q33 leads to qter
4 ring
5p Trisomy
5q3 Trisomy
5q33 to qter
5p Monosomy Ôåíîòèï. Ìèêðîöåôàëèÿ èëè ãîëîïðîçýíöåôàëèÿ, îêðóãëîå ëèöî, ãèïåðòåëîðèçì, ìèêðîãíàòèÿ, ïàòîëîãèÿ æåëóäî÷íî-êèøå÷íîãî òðàêòà (àòðåçèÿ ïèùåâîäà) óìñòâåííàÿ îòñòàëîñòü (IQ=20).
deletion of the short arm of chromosome 5
6p Trisomy
6p2 Trisomy
6q2 Trisomy
Duplication 7p with t(7;11)

91. WebGuest - Open Directory : Health : Conditions And Diseases : Genetic Disorders
Top Health Conditions and Diseases Genetic Disorders Pallister Killian MosaicSyndrome (3). See also Health Conditions and Diseases Rare Disorders (128).
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