Hawkinsinuria

You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.

Jump to: navigation, search
Hawkinsinuria
Classification and external resources
Hawkinsin
OMIM 276710 140350
DiseasesDB 29836
MeSH D020176

WikiDoc Resources for

Hawkinsinuria

Articles

Most recent articles on Hawkinsinuria

Most cited articles on Hawkinsinuria

Review articles on Hawkinsinuria

Articles on Hawkinsinuria in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Hawkinsinuria

Images of Hawkinsinuria

Photos of Hawkinsinuria

Podcasts & MP3s on Hawkinsinuria

Videos on Hawkinsinuria

Evidence Based Medicine

Cochrane Collaboration on Hawkinsinuria

Bandolier on Hawkinsinuria

TRIP on Hawkinsinuria

Clinical Trials

Ongoing Trials on Hawkinsinuria at Clinical Trials.gov

Trial results on Hawkinsinuria

Clinical Trials on Hawkinsinuria at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Hawkinsinuria

NICE Guidance on Hawkinsinuria

NHS PRODIGY Guidance

FDA on Hawkinsinuria

CDC on Hawkinsinuria

Books

Books on Hawkinsinuria

News

Hawkinsinuria in the news

Be alerted to news on Hawkinsinuria

News trends on Hawkinsinuria

Commentary

Blogs on Hawkinsinuria

Definitions

Definitions of Hawkinsinuria

Patient Resources / Community

Patient resources on Hawkinsinuria

Discussion groups on Hawkinsinuria

Patient Handouts on Hawkinsinuria

Directions to Hospitals Treating Hawkinsinuria

Risk calculators and risk factors for Hawkinsinuria

Healthcare Provider Resources

Symptoms of Hawkinsinuria

Causes & Risk Factors for Hawkinsinuria

Diagnostic studies for Hawkinsinuria

Treatment of Hawkinsinuria

Continuing Medical Education (CME)

CME Programs on Hawkinsinuria

International

Hawkinsinuria en Espanol

Hawkinsinuria en Francais

Businness

Hawkinsinuria in the Marketplace

Patents on Hawkinsinuria

Experimental / Informatics

List of terms related to Hawkinsinuria

Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.

Hawkinsinuria, also called 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, is an autosomal dominant metabolic disorder affecting the metabolism of the sulfur amino acid hawkinsin.[1]

It is characterized by transient metabolic acidosis and tyrosinemia.

Hawkinsinuria has an autosomal dominant pattern of inheritance.
Hawkinsinuria has an autosomal dominant pattern of inheritance.

See also

References


WikiDoc Help Menu

Quick Start..

Editing basics

Advanced editing

Communicating your edits

Help Videos You Can Watch


Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

Personal tools