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This Concept Map, created with IHMC CmapTools, has information related to: V28. Turner Syndrome, X Chroosome needed for misc upkeep, 28. TURNER SYNDROME inheritance risk Small familial pattern, 28. TURNER SYNDROME phenotype Bicuspid Aortic Valve, 28. TURNER SYNDROME Etiology 50 % 45, X, Complications include CV Disease, Normal intellectual development if present usually linked to 25% Structural abnormality, 28. TURNER SYNDROME Treatment Monitoring/ followup, In vitro fertilization if Infertile (Vast Majority), misc upkeep such as Renal Function, Growth Hormone if Below 5th ptile, 28. TURNER SYNDROME Etiology Between 1/2000 and 1/5000 live births, 28. TURNER SYNDROME Treatment In vitro fertilization, 28. TURNER SYNDROME Etiology 25% Structural abnormality, misc upkeep such as Hearing, 28. TURNER SYNDROME Phenotype Incomplete or absence, Normal intellectual development although Shy/withdrawn, 28. TURNER SYNDROME Etiology Incomplete or absence, Incomplete or absence of X Chroosome, 25% Mosiac likely caused by Loss of sex chromosome in early embryo, 28. TURNER SYNDROME phenotype Normal intellectual development