Have a symptom?
See what questions
a doctor would ask.

What is Beta-hydroxybutyric aciduria?

What is Beta-hydroxybutyric aciduria?

  • Beta-hydroxybutyric aciduria: A rare disorder of amino acid metabolism where glycine and proline are unable to be metabolized properly due to deficiency of the enzyme called succinic semialdehyde dehydrogenase.

Beta-hydroxybutyric aciduria: Introduction

Types of Beta-hydroxybutyric aciduria:

Broader types of Beta-hydroxybutyric aciduria:

What causes Beta-hydroxybutyric aciduria?

Causes of Beta-hydroxybutyric aciduria: see causes of Beta-hydroxybutyric aciduria

What are the symptoms of Beta-hydroxybutyric aciduria?

Symptoms of Beta-hydroxybutyric aciduria: see symptoms of Beta-hydroxybutyric aciduria

Beta-hydroxybutyric aciduria: Testing

Diagnostic testing: see tests for Beta-hydroxybutyric aciduria.

Misdiagnosis: see misdiagnosis and Beta-hydroxybutyric aciduria.

How is it treated?

Doctors and Medical Specialists for Beta-hydroxybutyric aciduria: Pediatrician ; see also doctors and medical specialists for Beta-hydroxybutyric aciduria.
Treatments for Beta-hydroxybutyric aciduria: see treatments for Beta-hydroxybutyric aciduria

Name of Beta-hydroxybutyric aciduria

Main name of condition: Beta-hydroxybutyric aciduria


By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise