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KTS

Introduction: KTS

Description of KTS

KTS (medical condition): A rare genetic disorder characterized by benign...more »

See also:

Klippel Trenaunay Weber syndrome:
  »Introduction: Klippel Trenaunay Weber syndrome
  »Symptoms of Klippel Trenaunay Weber syndrome

KTS: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

KTS is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that KTS, or a subtype of KTS, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

KTS as a Disease

KTS: Another name for Klippel Trenaunay Weber syndrome (or close medical condition association).
  »Introduction: Klippel Trenaunay Weber syndrome
  »Symptoms of Klippel Trenaunay Weber syndrome

KTS: Related Diseases

KTS: KTS is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of KTS (Klippel Trenaunay Weber syndrome)

Some of the symptoms of KTS incude:

  • Limb hypertrophy
  • Leg hypertrophy
  • Vascular lesions
  • Capiallary hemangiomas
  • Cavernous hemangiomas

KTS: Related Disease Topics

These medical disease topics may be related to KTS:

Terms associated with KTS:

Terms Similar to KTS:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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