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Holt-Oram Syndrome

Holt-Oram Syndrome: Introduction

Holt-Oram Syndrome: A rare inherited disorder characterized by hand, arm and heart abnormalities. Bone abnormalities usually affect the left arm more than the right and occasionally only one arm and/or hand is affected. More detailed information about the symptoms, causes, and treatments of Holt-Oram Syndrome is available below.

Symptoms of Holt-Oram Syndrome

Home Diagnostic Testing

Home medical testing related to Holt-Oram Syndrome:

Wrongly Diagnosed with Holt-Oram Syndrome?

Holt-Oram Syndrome: Related Patient Stories

Holt-Oram Syndrome: Complications

Read more about complications of Holt-Oram Syndrome.

Causes of Holt-Oram Syndrome

Read more about causes of Holt-Oram Syndrome.

Disease Topics Related To Holt-Oram Syndrome

Research the causes of these diseases that are similar to, or related to, Holt-Oram Syndrome:

Less Common Symptoms of Holt-Oram Syndrome

Holt-Oram Syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Holt-Oram Syndrome

Heart attacks can be undiagnosed: Although the most severe symptoms of heart attack are hard to miss, there are varying degrees of severity. It is altogether too common for people to die from undiagnosed heart attack, or from...read more »

Heart attacks can be overdiagnosed: Although many people die from heart attacks, there are also many cases where people fear that they have a heart attack, but actually have something milder. Some of the...read more »

Rare heart condition often undiagnosed: The rare heart condition called long QT syndrome can lead to episodes of palpitations and rapid heartbeat. In rare...read more »

Heart attack can be over-diagnosed: Although heart attack is often undiagnosed, leading to fatality, it can also be over-diagnosed. People become concerned that...read more »

Blood pressure cuffs misdiagnose hypertension in children: One known misdiagnosis issue with hyperension, arises in relation to the simple equipment used to test blood pressure. The "cuff" around...read more »

Hypertension misdiagnosis common in children: Hypertension is often misdiagnosed in adults (see misdiagnosis of hypertension), but its misdiagnosis is even more likely in...read more »

Holt-Oram Syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Holt-Oram Syndrome

Research quality ratings and patient safety measures for medical facilities in specialties related to Holt-Oram Syndrome:

Choosing the Best Hospital: More general information, not necessarily in relation to Holt-Oram Syndrome, on hospital performance and surgical care quality:

Holt-Oram Syndrome: Rare Types

Rare types of diseases and disorders in related medical categories:

Evidence Based Medicine Research for Holt-Oram Syndrome

Medical research articles related to Holt-Oram Syndrome include:

Click here to find more evidence-based articles on the TRIP Database

Holt-Oram Syndrome: Animations

Research about Holt-Oram Syndrome

Visit our research pages for current research about Holt-Oram Syndrome treatments.

Statistics for Holt-Oram Syndrome

Holt-Oram Syndrome: Broader Related Topics

User Interactive Forums

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Definitions of Holt-Oram Syndrome:

Characterized by malformations of bones of the thumbs, hands and forearms and/or abnormalities of the heart; in many infants, the thumbs and wrists may be absent, underdeveloped or have an extra bone; scapulae, clavicles, and/or other bones may also be abnormal. - (Source - Diseases Database)

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

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Holt-Oram Syndrome as a "rare disease".
Source - Orphanet

 

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