SADDAN

Introduction: SADDAN

Description of SADDAN

SADDAN (medical condition): A very rare inherited disorder characterized by abnormal bone development and brain and skin abnormalities.

See also:

Severe achondroplasia with developmental delay and acanthosis nigricans:
  »Introduction: Severe achondroplasia with developmental delay and acanthosis nigricans
  »Symptoms of Severe achondroplasia with developmental delay and acanthosis nigricans

SADDAN: Rare Disease

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

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

SADDAN as a Disease

SADDAN: Another name for Severe achondroplasia with developmental delay and acanthosis nigricans (or close medical condition association).
  »Introduction: Severe achondroplasia with developmental delay and acanthosis nigricans
  »Symptoms of Severe achondroplasia with developmental delay and acanthosis nigricans

Symptoms of SADDAN (Severe achondroplasia with developmental delay and acanthosis nigricans)

Some of the symptoms of SADDAN incude:

• Very short stature
• Short arms
• Short legs
• Bowed leg bones
• Small chest

See full list of 18 symptoms of SADDAN (Severe achondroplasia with developmental delay and acanthosis nigricans)

Terms associated with SADDAN:

Terms Similar to SADDAN:

• SADDAN dysplasia
• SSB syndrome
• Skeleton-skin-brain syndrome
• Severe achondroplasia with developmental delay and acanthosis nigricans

Source - NIH

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

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