DINO - Language: Englisch - Health - Conditions And Diseases - F Translate this page Dieser Link verweist auf eine Haupt-Kategorie Facial Paralysis Dieser Link verweistauf eine Haupt-Kategorie faciocutaneoskeletal syndrome Dieser Link verweist http://www.dino-online.de/dino_page_7d2196c29790afabc10cc0762522531b.html
Vindex, De Vindplaats Van Het Nederlandse Web Fabry's Disease@ Facial Differences@ Facial Paralysis@ faciocutaneoskeletal syndrome@Faciogenitopopliteal Syndrome@ Factititious Disorders@ Factor V Leiden http://www.vindex.nl/dir/Health/Conditions_and_Diseases/F
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Extractions: Pathologists use lots of abbreviations and acronyms. An acronym is an abbreviation of a phrase, where each letter of the acronym is added consecutively from the first letter of each of the words of the phrase. An abbreviation is a shortened form of a text-string, and all acronyms are types of abbreviations.
Euskaraz.net - Top honek editorea behar du. Fabry's Disease@ (8); Facial Differences@(85); Facial Paralysis@ (40); faciocutaneoskeletal syndrome@ (3); http://www.euskaraz.net/Loturak/Top/Health/Conditions_and_Diseases/F/
F Top Health Conditions and Diseases F (0) Fabry's Disease@ (8); Facial Differences@(90); Facial Paralysis@ (40); faciocutaneoskeletal syndrome@ (3); http://www.linkspider.biz/Health/ConditionsandDiseases/F/
Freenet.de Suche - Language: Englisch - Health - Conditions And Diseases - F Translate this page , Facial Differences. , Facial Paralysis. , faciocutaneoskeletal syndrome., Faciogenitopopliteal Syndrome. , Factititious Disorders. , Factor V Leiden. http://webkatalog.freenet.de/freenet_page_7d2196c29790afabc10cc0762522531b.html
Wishbone.com - Start Searching! Top Health Conditions_and_Diseases F. Fabry's Disease@; Facial Differences@;Facial Paralysis@; faciocutaneoskeletal syndrome@; Faciogenitopopliteal http://wishbone.com/Health/Conditions_and_Diseases/F
Extractions: Syndrome Costello syndrome Synonym faciocutaneoskeletal (FCS) syndrome Summary Retarded growth and mental development, coarse facies, nasal papillomata, cutis laxa of the hands and feet, and other abnormalities. Major Features Head and neck: Macrocephaly, coarse facies, large fontanels or delayed closure and wide and long forehead. Papillomata around the mouth and nares. Ears: Low-set ears with thick lobes. Eyes: Downslanting palpebral fissures and strabismus. Nose: Depressed nasal bridge and epicanthal folds. Mouth and oral structures: Wide and large mouth with thick lips, macroglossia, highly arched palate, and tooth enamel dysplasia. Neck: Short neck. Thorax: Barrel chest. Abdomen: Hernia. Hand and foot: Hyperkeratosis palmaris et plantaris, palmar nevi, short and flat hyperextensible fingers, ulnar deviation of hands, and positional defects of the feet. Dermatoglyphic findings consist of deep plantar and palmar creases. Extremities: Tight Achilles tendon and defective elbow extension.
Birth Disorder Information Directory - F Facioauriculovertebral (FAV) Sequence See Goldenhar (Gorlin) syndrome. faciocutaneoskeletal(FCS) syndrome See Costello syndrome. Faciogenital Dysplasia http://www.bdid.com/defectf.htm
Extractions: HOME F Syndrome F Form of Acropectorovertebral Dysplasia Fabry Disease Facial Asymmetry/Hemihypertrophy Facial Palsy Facioaudiosymphalangism Syndrome F acio a uriculo v ertebral ( FAV ) Sequence F acio c utaneo s keletal ( FCS ) Syndrome Faciogenital Dysplasia Faciodigitogenital Syndrome Faciogenitopopliteal Syndrome (Popliteal Pterygium Syndrome) Faciopalatoosseous Syndrome Facioscapulohumeral Muscular Dystrophy (FSH, Landouzy-Dejerine Dystrophy) Factor XI Deficiency Fahr Disease (Basal Ganglia Calcification, Idiopathic; Cerebral Calcification, Nonarteriosclerotic; Ferrocalcinosis, Cerebrovascular; S trio p alli d odentate [ SPD ] Calcinosis) Fairbank's Disease Familial Atypical Mole-Malignant Melanoma Syndrome See Melanoma, Familial/Cutaneous Malignant Type
Reference Page 2 with a previously undefined multiple congenital anomalies/mental retardation (MCA/MR)syndrome which they designated the faciocutaneoskeletal (FCS) syndrome. http://www.costellokids.co.uk/ref2.htm
Extractions: Borochowitz et al. (1992) reported 5 unrelated patients, 1 male and 4 females, with a previously undefined multiple congenital anomalies/mental retardation (MCA/MR) syndrome which they designated the faciocutaneoskeletal (FCS) syndrome. The features included mental retardation with specific sociable, humorous behavior, characteristic facial appearance, generally excessive skin, postnatal growth failure, and skeletal abnormalities. Consanguinity was noted in 2 patients, suggesting autosomal recessive inheritance. Coarse facies, wide hirsute forehead, wide anteverted nostrils, and thick lips were pictured. Martin and Jones (1993), Der Kaloustian (1993), Teebi (1993), Philip and Mancini (1993), and Zampino et al. (1993) suggested that the FCS syndrome described by Borochowitz et al. (1992) is the same as the Costello syndrome. Borochowitz et al. (1993) concluded, on the other hand, that 'it is premature to reach a definite conclusion at this stage.' Patton and Baraitser (1993) reviewed 5 cases from their previous paper on cutis laxa (Patton et al., 1987) and concluded that the appropriate diagnosis was in fact Costello syndrome. Independently, Davies and Hughes (1994) reviewed case 7 from the same paper and, based on both history and clinical examination, made 'an unequivocal diagnosis of Costello syndrome.' In a longer report, Davies and Hughes (1994) described the development of one of the patients of Patton et al. (1987) for more than 10 years and again emphasized that Costello syndrome should be included in the differential diagnosis of cutis laxa in association with postnatal growth retardation and developmental delay. Fryns et al. (1994) described 2 unrelated patients with Costello syndrome, a 12-year-old girl and a 3.5-year-old boy. Severe postnatal growth retardation was the first clinical sign. Characteristic facial changes, loose and hyperelastic skin, and papillomata became progressively more evident with age. The patients presented a pleasant, happy nature and were mildly to moderately mentally retarded. Okamoto et al. (1994) reported the case of a Japanese patient. A fundoplication was performed at the age of 11 months to treat severe gastroesophageal reflux. The infant had congenital bilateral subluxation of the hips. At the age of 7 years, there was generalized pigmentation and acanthosis nigricans around the neck and axilla. Endocrinologic evaluation demonstrated partial deficiency of growth hormone. Stating that 16 cases had been reported, Torrelo et al. (1995) presented the case of a 15-year-old girl and emphasized the cutaneous manifestations of the disorder.
Malattie Rare E Genetiche Lettera "F" Translate this page melica, sindromeFacio cardio melique syndrome{} * Facio-cutaneo-scheletricaSindromeFCSfaciocutaneoskeletal (FCS) syndromeFacio Cutáneo http://utenti.lycos.it/fmfpc/F.htm
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1Up Health > Health Links Directory > Conditions And Diseases: F Fabry's Disease (8) Facial Differences (85) Facial Paralysis (40) Faciocutaneoskeletalsyndrome (3) Faciogenitopopliteal syndrome (2) Factititious Disorders (13 http://www.1uphealth.com/links/conditions-and-diseases-f.html
Extractions: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites. Home Contact Us Privacy Links Directory
Costello Syndrome AD.COM Web Directory, search, Costello syndrome. Top Health Conditions_and_Diseases Genetic_Disorders Costello_syndrome 2, NORD Costello syndrome. http://www.ad.com/Health/Conditions_and_Diseases/F/__Faciocutaneoskeletal_Syndro
