KCS1

Introduction: KCS1

Description of KCS1

KCS1 (medical condition): A very rare inherited skeletal disorder involving thickening of the long...more »

See also:

Kenny-Caffey syndrome, Type 1:
  »Introduction: Kenny-Caffey syndrome, Type 1
  »Symptoms of Kenny-Caffey syndrome, Type 1

KCS1: Rare Disease

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

KCS1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that KCS1, or a subtype of KCS1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

KCS1 as a Disease

KCS1: Another name for Kenny-Caffey syndrome, Type 1 (or close medical condition association).
  »Introduction: Kenny-Caffey syndrome, Type 1
  »Symptoms of Kenny-Caffey syndrome, Type 1

KCS1: Related Diseases

KCS1: KCS1 is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Bone or skeletal conditions
• Musculoskeletal conditions
• Limb conditions
• Head conditions

Symptoms of KCS1 (Kenny-Caffey syndrome, Type 1)

Some of the symptoms of KCS1 incude:

• Tetanic convulsions
• Delayed physical development
• Myopia
• Small eyes
• Farsightedness

See full list of 23 symptoms of KCS1 (Kenny-Caffey syndrome, Type 1)

KCS1: Related Disease Topics

These medical disease topics may be related to KCS1:

• rare inherited skeletal disorder
• tetanic convulsions
• micropthalmia
• hypermetropia

Terms associated with KCS1:

Terms Similar to KCS1:

• Kenny-Caffey syndrome, autosomal recessive form
• Kenny-Caffey syndrome, Type 1

Source - NIH

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