AHDS

Introduction: AHDS

Description of AHDS

AHDS (medical condition): A very rare inherited disorder characterized...more »

See also:

Allan-Herndon-Dudley Syndrome:
  »Introduction: Allan-Herndon-Dudley Syndrome
  »Symptoms of Allan-Herndon-Dudley Syndrome

AHDS: Rare Disease

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

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

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list AHDS as a "rare disease".

Source - Orphanet

AHDS as a Disease

AHDS: Another name for Allan-Herndon-Dudley Syndrome (or close medical condition association).
  »Introduction: Allan-Herndon-Dudley Syndrome
  »Symptoms of Allan-Herndon-Dudley Syndrome

AHDS: Related Diseases

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

• Genetic conditions
• Mental retardation conditions
• Intellectual or developmental disabilities
• Musculoskeletal conditions
• Neuromuscular conditions
• Muscle conditions

Symptoms of AHDS (Allan-Herndon-Dudley Syndrome)

Some of the symptoms of AHDS incude:

• Hypotonia
• Unable to hold up head at 6 months
• Speaking difficulty
• Impaired ability to control voluntary movements
• Athetoid movements

See full list of 18 symptoms of AHDS (Allan-Herndon-Dudley Syndrome)

AHDS: Related Disease Topics

These medical disease topics may be related to AHDS:

• brain development disorder
• hypotonia
• muscle hypoplasia
• spasticity

Terms associated with AHDS:

Terms Similar to AHDS:

• Allan-Herndon syndrome
• Allan-Herndon-Dudley syndrome
• Mental retardation and muscular atrophy
• Mental retardation, X-linked, with hypotonia
• X-linked mental retardation-hypotonia

Source - NIH

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