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81. Facial Differences At Product-Magazine
Iplexx Directory Health Support Groups Conditions and Diseases Facial Differences langergiedion syndrome Health Support Groups Conditions and
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82. Langer-Giedion, Syndrome : Arborescences MeSH
Translate this page langer-giedion, syndrome arborescences MeSH. Menu général CISMeF. Vous pouvez aussi consulter toutes les arborescences des mots
http://www.chu-rouen.fr/navimesh/L/navilangergiedionsyndrome.html
Langer-Giedion, syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF

83. ORPHANET® : Langer-Giedion, Syndrome De
Translate this page ORPHANET. Accès à la base de données Orphanet. langer-giedion, syndrome de. Accès direct aux détails Résumé Le syndrome de Langer
http://www.orpha.net/static/FR/langergiedion.html
Accès à la base de données Orphanet
Langer-Giedion, syndrome de
Accès direct aux détails Résumé
Le syndrome de Langer-Giedion est caractérisé par un nez bulbeux, des oreilles décollées, des cheveux clairsemés, des épiphyses en cône au niveau des phalanges, des exostoses cartilagineuses multiples et un retard mental léger ou modéré. Sa transmission est autosomique dominante. Il est dû à une microdélétion chromosomique de la région 8q23.3-q24.13 entraînant la perte d'au moins deux gènes : et . *Auteur : Dr S. Aymé (septembre 2002)*. Signes de la maladie
  • ARC CUPIDON ABSENT/PHILTRUM PLAT-LARGE
  • DELETION CHROMOSOMIQUE SUB-MICROSCOPIQUE
  • EPIPHYSES EN CONE
  • EXOSTOSES
  • LEVRES MINCES/RETRACTEES
  • MICROCEPHALIE
  • OREILLES DECOLLEES/PROEMINENTES
  • PHILTRUM LONG
  • RETARD MENTAL MODERE / LEGER
  • SOURCILS CLAIRSEMES/ABSENTS/FINS
  • ASYMETRIE CORPORELLE / HEMITROPHIE
  • CHEVEUX RARES/HYPOTRICHIE/ATRICHIE
  • DENTS MAL IMPLANTEES
  • ENOPHTALMIE
  • FENTE PALPEBRALE ANTIMONGOLOIDE
  • HYPERTELORISME
  • MACROSTOMIE/GRANDE BOUCHE
  • MAINS COURTES/BRACHYDACTYLIE
  • NEZ LARGE/ARETE NASALE LARGE
  • NEZ LONG/GROS/EN BULBE
  • OMOPLATE ANOMALIE
  • ONGLES FINS / HYPOPLASIQUES (PIEDS)
  • ONGLES FINS/HYPOPLASIQUES (MAINS)
  • OREILLE GRANDE/LONGUE/LARGE
  • PETITE TAILLE / NANISME
  • TRISOMIE OU MONOSOMIE TOTALE/PARTIELLE
  • CLINODACTYLIE DU 5EME DOIGT
  • FACE ETROITE
  • FRONT LARGE
  • HEMIVERTEBRES/FUSIONS VERTEBRALES
  • HYPERLAXITE LIGAMENTAIRE
  • LEVRES EPAISSES
  • NAEVI PIGMENTES
  • OREILLES BAS IMPLANTEES
  • PALAIS OGIVAL/ETROIT
  • PEAU HYPERELASTICITE
  • PIED BOT VARUS/VALGUS
  • SCOLIOSE
  • SPINA BIFIDA OCCULTA
  • STRABISME
  • THORAX ETROIT
Mise à jour : 01/06/2004

84. LANGER-GIEDION (TRICHO-RHINO-PHALANGEAL) SYNDROME
Features Listed For langergiedion (TRICHO-RHINO-PHALANGEAL) syndrome. McKusick 150230. Abdominal muscle hypoplasia/aplasia; Cartilaginous
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?971

85. Craniofacial Syndrome - Encyclopedia Article About Craniofacial Syndrome. Free A
Craniofacial syndrome. 22 q11 microdeletion syndrome is a birth defect A birth defect is a physical or mental abnormality present at the time a child is born.
http://encyclopedia.thefreedictionary.com/Craniofacial syndrome
Dictionaries: General Computing Medical Legal Encyclopedia
Craniofacial syndrome
Word: Word Starts with Ends with Definition 22 q11 microdeletion syndrome is a birth defect A birth defect is a physical or mental abnormality present at the time a child is born. Birth defects range from minimal, such as birthmarks, and slightly mobility-impairing, such as amelia of the legs, to very serious, such as cerebral palsy, and incompatible with life, such as anencephaly. Many birth defects result from genetic abnormalities. Others can arise from chance problems in fetal development (teratogenesis), which are sometimes caused by prenatal vitamin deficiencies or exposure to mercury and other harmful substances.
Click the link for more information. caused by a genetic The word " gene " is shared by many disciplines, including whole organism-based or classical genetics, molecular genetics, evolutionary biology and population genetics. It has multiple uses within each of these contexts, but in the primary sense, genes are material things that parents pass to offspring during reproduction; these things encode information essential for the construction and regulation of polypeptides, proteins and other molecules essential for the growth and functioning of the organism. This sense, which is common to all of the above disciplines, is also the original historical meaning of gene.
Click the link for more information.

86. Langer Giedion Syndrome
Browse entry words starting with A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y, Z, Other characters, Langer giedion syndrome,. Print this article,
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/LANGER GIEDION
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Langer giedion syndrome, (Leonard Langer, 20th century, American paediatric radiologist; Andreas Giedion, 20th century, Swiss paediatric radiologist). Clinically the patients appear similar to trichorhinophalangeal dysplasia Type I but have in addition short stature and mental retardation. Radiographically, in addition to the features seen in Type I, there are multiple cartilaginous exostoses.
HC
The Encyclopaedia of Medical Imaging Volume VII
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87. Langer – Giedion Syndrome
Browse entry words starting with A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y, Z, Other characters, Langer – giedion syndrome,. Print this article,
http://www.amershamhealth.com/medcyclopaedia/Volume VII/LANGER GIEDION SYNDROME
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Langer – giedion syndrome, (Leonard Langer, 20th century, American paediatric radiologist; Andreas Giedion, 20th century, Swiss paediatric radiologist). Clinically the patients appear similar to trichorhinophalangeal dysplasia Type I but have in addition short stature and mental retardation. Radiographically, in addition to the features seen in Type I, there are multiple cartilaginous exostoses.
HC
The Encyclopaedia of Medical Imaging Volume VII Contacts GE Healthcare Making Waves

88. Langer Giedion Syndrome
Back Home Next. Langer Giedion syndrome. The Wells Lab Langer Giedion syndrome Home Page. Copyright of Ability All Rights Reserved1990 Webmaster .
http://www.ability.org.uk/Langer_Giedion_Syndrome.html
Our Aims Services Stats ... Z Langer Giedion Syndrome Langer-Giedion Syndrome Association - An international network of families and professionals dedicated to providing information and support to people. The Wells Lab Langer Giedion Syndrome Home Page Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

89. Birth Disorder Information Directory - L
LandouzyDejerine Dystrophy See Facioscapulohumeral Muscular Dystrophy. Langer Giedion syndrome (Trichorhinophalangeal syndrome, Type II)
http://www.bdid.com/defectl.htm

HOME
L
Laband Syndrome Lacrimal Duct Defect Lacrimoauriculodentodigital Syndrome (Levy Hollister Syndrome) Lacunar Skull Ladda Zonana Ramer Syndrome (Contractures Ectodermal Dysplasia Cleft Lip Palate) Lambert Syndrome (Branchial Dysplasia Mental Retardation Inguinal Hernia) Landings Disease (GM 1 gangliosidosis) Landouzy-Dejerine Dystrophy Langer Giedion Syndrome (Trichorhinophalangeal Syndrome, Type II) Langer Mesomelic Dysplasia (Dyschondrosteosis, Homozygous; Mesomelic Dwarfism of the Hypoplastic Ulna, Fibula, and Mandible Type) Langer Nishino Yamaguchi Syndrome (Brachymesomelia Renal Syndrome) Laron Syndrome (Pituitary Dwarfism II) Larsen Syndrome

90. Canadian Directory Of Genetic Support Groups
Langer Giedion syndrome Association Louise Kinross LGSA Cofounder 89 Ingham Avenue Toronto, Ontario, Canada, M4K 2W8 Tel 416.465.3029 Fax 416.465.4963
http://www.lhsc.on.ca/programs/medgenet/langergi.htm

Index by
support group Canadian Directory of Genetic Support Groups
Langer Giedion Syndrome Association
Louise Kinross LGSA Co-founder
89 Ingham Avenue
Toronto, Ontario, Canada, M4K 2W8
Tel: 416.465.3029
Fax: 416.465.4963
Website: Langer Giedion Syndrome Association Page revised:July 30, 2002 Maintained by: Janice Little
Index by disease/ disorder

Return to Programs and Services Questions? Comments? Contact Janice Little London Health Sciences Centre . Please read our

91. Redirect

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92. Gimenei >> Health >> Support_Groups >> Conditions_and_Diseases >> Facial_Differe
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Health Support Groups Conditions and Diseases ... Facial Differences Langer Giedion Syndrome Music: Tabula Rasa
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