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AATD

Introduction: AATD

Description of AATD

AATD (medical condition): Alpha-1 antitrypsin deficiency is an inherited disorder that can...more »

See also:

Homozygotic Alpha 1 antitrypsin Defeciency:
  »Introduction: Homozygotic Alpha 1 antitrypsin Defeciency
  »Symptoms of Homozygotic Alpha 1 antitrypsin Defeciency
  »Causes of Homozygotic Alpha 1 antitrypsin Defeciency
  »Treatments for Homozygotic Alpha 1 antitrypsin Defeciency

AATD as a Disease

AATD: Another name for Homozygotic Alpha 1 antitrypsin Defeciency (or close medical condition association).
  »Introduction: Homozygotic Alpha 1 antitrypsin Defeciency
  »Symptoms of Homozygotic Alpha 1 antitrypsin Defeciency
  »Causes of Homozygotic Alpha 1 antitrypsin Defeciency
  »Treatments for Homozygotic Alpha 1 antitrypsin Defeciency

AATD: Related Diseases

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

Causes of AATD

Some of the causes of AATD are included in the list below:

  • Genetic mutation

Symptoms of AATD (Homozygotic Alpha 1 antitrypsin Defeciency)

Some of the symptoms of AATD incude:

Treatments for AATD (Homozygotic Alpha 1 antitrypsin Defeciency)

Treatments for AATD (Homozygotic Alpha 1 antitrypsin Defeciency) include:

  • Replacement or Augmentation therapy- intravenous infusions of alpha-1 antitrypsin

Treatment of AATD: For more treatment information about AATD, see treatment of Homozygotic Alpha 1 antitrypsin Defeciency (AATD)

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