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Monday, February 13, 2012

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Williams Syndrome Learning Center

Williams syndrome is a rare genetic disorder that can lead to problems with development.

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Williams Syndrome Causes

Gene Mutation

Tests

Physical Therapy
Speech Therapy
Avoid Extra Calcium and Vitamin D

Available Treatments

Williams Syndrome Details

Complications

Prenatal Testing

Doctor Specialties

News

Gene Linked to Separation Anxiety
WEDNESDAY, Nov. 16 (HealthDay News) -- Scientists who identified a gene linked ...
Kids With Rare Condition Lack Racial Prejudice
TUESDAY, April 13 (HealthDay News) -- Children with a rare condition called Wil...

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Congenital chromosomal disease

22q13 Deletion Syndrome, Chromosome Abnormality, Cornelia De Lange Syndrome, Edward's Syndrome, Fragile X Syndrome, Patau Syndrome, Prader-Willi Syndrome, Rubinstein Taybi Syndrome, Williams Syndrome

Mental Retardation

Cornelia De Lange Syndrome, Mild Mental Retardation, Prader-Willi Syndrome, Williams Syndrome

Congenital Disorders

Birth Defects, Congenital Adrenal Hyperplasia, Congenital lactase deficiency, Congenital Limb Abnormalities, Congenital Myasthenia, Congenital Reproductive System Disorder, Erythropoietic porphyria, Hereditary Elliptocytosis, Inborn Errors of Metabolism, Kallmann Syndrome, Klippel-Feil Syndrome, Leber's Amaurosis, Myotonia Congenita, Prader-Willi Syndrome, more »

Williams Syndrome Learning Center

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Congenital chromosomal disease

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Congenital Disorders

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Williams Syndrome Learning Center

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Williams Syndrome Causes

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Williams Syndrome Details

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