Three M syndrome

Introduction: Three M syndrome

Description of Three M syndrome

Three M syndrome (medical condition): A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected.

See also:

3-M Syndrome:
  »Introduction: 3-M Syndrome
  »Symptoms of 3-M Syndrome

Three M syndrome: Rare Disease

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

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

Three M syndrome as a Disease

Three M syndrome: Another name for 3-M Syndrome (or close medical condition association).
  »Introduction: 3-M Syndrome
  »Symptoms of 3-M Syndrome

Symptoms of Three M syndrome (3-M Syndrome)

Some of the symptoms of Three M syndrome incude:

• Growth retardation
• Fetal growth retardation
• Short wide neck
• Prominent upper back muscles
• Breast bone deformity

See full list of 26 symptoms of Three M syndrome (3-M Syndrome)

Terms associated with Three M syndrome:

Terms Similar to Three M syndrome:

• 3M syndrome

Source: Diseases Database

• 3M syndrome
• Dolichospondylic dysplasia

Source - NIH

External links related to: Three M syndrome

• NORD - National Organization for Rare Disorders, Inc.
• OMIM - THREE M SYNDROME
• GeneReviews: 3-M Syndrome

Source: Diseases Database

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

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