What is Daneman Davy Mancer syndrome?

What is Daneman Davy Mancer syndrome?

• Daneman Davy Mancer syndrome: A very rare syndrome characterized mainly by kidney, thyroid and finger and toe abnormalities.

Daneman Davy Mancer syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Daneman Davy Mancer syndrome, or a subtype of Daneman Davy Mancer 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 Daneman Davy Mancer syndrome as a "rare disease".
Source - Orphanet

Daneman Davy Mancer syndrome: Introduction

Types of Daneman Davy Mancer syndrome:

Broader types of Daneman Davy Mancer syndrome:

• Kidney conditions
• Urinary system conditions
• Liver conditions
• Hand conditions
• Foot conditions
• Musculoskeletal conditions
• Limb conditions
• Bone or skeletal conditions
• Congenital conditions - physical defects
• Congenital conditions
• more types...»

What causes Daneman Davy Mancer syndrome?

Causes of Daneman Davy Mancer syndrome: see causes of Daneman Davy Mancer syndrome

What are the symptoms of Daneman Davy Mancer syndrome?

Symptoms of Daneman Davy Mancer syndrome: see symptoms of Daneman Davy Mancer syndrome

Daneman Davy Mancer syndrome: Testing

Diagnostic testing: see tests for Daneman Davy Mancer syndrome.

Misdiagnosis: see misdiagnosis and Daneman Davy Mancer syndrome.

How is it treated?

Doctors and Medical Specialists for Daneman Davy Mancer syndrome: Pediatrician, Endocrinologist ; see also doctors and medical specialists for Daneman Davy Mancer syndrome.
Treatments for Daneman Davy Mancer syndrome: see treatments for Daneman Davy Mancer syndrome

Name and Aliases of Daneman Davy Mancer syndrome

Main name of condition: Daneman Davy Mancer syndrome

Multinodular goiter cystic kidney polydactyly, thyroid [renal - digital anomalies], Multinodular goiter, cystic renal disease, and digital anomalies, MNG/CRD/DA

MNG/CRD/DA, Multinodular goiter, cystic renal disease, and digital anomalies
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

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