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Disease Information for Oculodentodigital dysplasia syndrome
- Clinical Manifestations
- Signs & Symptoms
- Particular physiognomy/Odd looking kids
- Craniofacial Abnormalities/Congenital
- Pinched/thin nose
- Dry brittle hair/Lank lifeless hair
- Slow Hair Growth
- Teeth malformed/dysplastic
- Webbed fourth and fifth fingers
- Narrow Nostrils
- Dysmorphic appearance/face
- Eye symptoms/signs
- Clinical Presentation & Variations
- Presentation/Multiple deformities newborn (odd look)
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
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- Population Group
- Child
- Population/Pediatrics population
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Associated Diseases & Rule outs
- Associated Disease & Complications
- Blindness in Children
- Dental deformities/anomalies
- Glaucoma
- Limb deformities/anomalies
- Microcornea
- Oculodentodigital dysplasia syndrome
- Syndactyly/Webbing
- Teeth enamel hypoplastic
- Webbed fingers or toes/congenital
- Hand anomalies
- Disease Mechanism & Classification
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Systemic/no comment (category)
- Pathophysiology
- Pathophysiology/Maternal Chromosome mutation
- Process
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Congenital/developmental (category)
- PROCESS/Dysplasia/aplasia (ex)
- PROCESS/Eponymic/Esoteric/Not yet integrated into database
- PROCESS/Genetic disorder/Spontaneous mutations/sporadic
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- Synonyms
- Synonym
- ANIRIDIA CEREBELLAR ATAXIA AND MENTAL DEFICIENCY, Curtius' syndrome, Curtius' syndrome I, dento oculo osseous dysplasia, dysplasia oculodentodigital, dysplasia oculodentodigitalis, Ectodermal dysplasia ocular malformation syndrome, Ectodermal dysplasia ocular malformation syndrome (disorder), Ectodermal dysplasia with ocular malformations syndrome, FIFTH PHACOMATOSIS, Meyer Schwinkerath and Weyers syndrome, Meyer Schwinkerath syndrome, MULTIPLE BASAL CELL NEVI ODONTOGENIC KERATOCYSTS AND SKELETAL ANOMALIES, oculo dento digital (ODD) dysplasia (ODDD), oculo dento digital (ODD) syndrome, oculo dento digital dysplasia, Oculo dento digital syndrome, oculo dento osseous dysplasia, oculo dento osseous dysplasia (ODOD), oculodentodigital dysplasia, OCULODENTODIGITAL DYSPLASIA SYNDROME, Oculodentodigital syndrome, Oculodentodigital syndrome (disorder), OCULODENTOOSSEOUS DYSPLASIA, ODD SYNDROME, ODDD, ODOD, osseous oculo dental dysplasia, Synonym/Meyer-Schwickerath syndrome, Synonym/ODD Syndrome, Synonym/ODOD Syndrome, Synonym/Osseous-Oculo-Dento dysplasia
- Definition
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Oculo Dento Digital Dysplasia; Dento-Oculo-Osseous Dysplasia; ODD Syndrome; ODOD; Oculo-Dento-Osseous Dysplasia; Osseous-Oculo-Dento Dysplasia; Oculo-Dento-Digital Dysplasia is a rare disorder that may be inherited as an autosomal dominant trait or be caused by a new change in the genes that occurs for no apparent reason (mutation); Major symptoms of Oculo-Dento-Digital Dysplasia are webbing of the fourth and fifth fingers, an abnormally small transparent part of the eye (microcornea), a slender nose with narrow nostrils, underdevelopment of the outer flaring wall of each nostril (alae), defective enamel and dry hair that grows slowly---------[NORD 2005]-------
(Edit)
- External Links Related to Oculodentodigital dysplasia syndrome
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)
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