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What is Von voss Cherstvoy syndrome?

What is Von voss Cherstvoy syndrome?

  • Von voss Cherstvoy syndrome: An early congenital condition that is characterised by multiple congenital anomalies.

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

Von voss Cherstvoy syndrome: Introduction

Types of Von voss Cherstvoy syndrome:

Broader types of Von voss Cherstvoy syndrome:

What causes Von voss Cherstvoy syndrome?

Causes of Von voss Cherstvoy syndrome: see causes of Von voss Cherstvoy syndrome

What are the symptoms of Von voss Cherstvoy syndrome?

Symptoms of Von voss Cherstvoy syndrome: see symptoms of Von voss Cherstvoy syndrome

Von voss Cherstvoy syndrome: Testing

Diagnostic testing: see tests for Von voss Cherstvoy syndrome.

Misdiagnosis: see misdiagnosis and Von voss Cherstvoy syndrome.

How is it treated?

Doctors and Medical Specialists for Von voss Cherstvoy syndrome: Pediatrician ; see also doctors and medical specialists for Von voss Cherstvoy syndrome.
Treatments for Von voss Cherstvoy syndrome: see treatments for Von voss Cherstvoy syndrome

Name and Aliases of Von voss Cherstvoy syndrome

Main name of condition: Von voss Cherstvoy syndrome

Other names or spellings for Von voss Cherstvoy syndrome:

Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies, Klippel-feil deformity, conductive deafness, and absent vagina, Dk phocomelia syndrome, Phocomelia [thrombocytopenia - encephalocele], Phocomelia thrombocytopenia encephalocele

Dk--phocomelia syndrome, MURCS association, Mullerian duct and renal agenesis with upper limb and rib anomalies, Mullerian-Renal-Cervicothoracic Somite Abnormalities, Phocomelia, thrombocytopenia, encephalocele, urogenital malformations
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Von voss Cherstvoy syndrome: Related Conditions

Research the causes of these diseases that are similar to, or related to, Von voss Cherstvoy syndrome:

 

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