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C Syndrome

C Syndrome: Introduction

C Syndrome: A rare inherited disorder characterized by a triangular-shaped head, facial anomalies, joint contractures and loose skin. More detailed information about the symptoms, causes, and treatments of C Syndrome is available below.

Symptoms of C Syndrome

Wrongly Diagnosed with C Syndrome?

C Syndrome: Complications

Read more about complications of C Syndrome.

Causes of C Syndrome

Read more about causes of C Syndrome.

Disease Topics Related To C Syndrome

Research the causes of these diseases that are similar to, or related to, C Syndrome:

Misdiagnosis and C Syndrome

Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer from the skin disorder called psoriasis can often go undiagnosed. The...read more »

Psoriatic arthritis often undiagnosed cause of joint conditions: Patients with the skin condition psoriasis can also have the related arthritis subtype called "psoriatic arthritis"....read more »

C Syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for C Syndrome

Medical research articles related to C Syndrome include:

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

C Syndrome: Animations

Research about C Syndrome

Visit our research pages for current research about C Syndrome treatments.

Statistics for C Syndrome

C Syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about C Syndrome, or answer someone else's question, on our message boards:

Definitions of C Syndrome:

A multiple congenital anomaly/mental retardation syndrome marked by trigonocephaly due to craniosynostosis, orofacial anomalies (mainly metopic prominence, upward slating of the palpebral fissures, epicanthal folds, hypoplastic nose, malformed ears, and abnormal palate) associated with various renal, pulmonary, genital, and cardiovascular defects. Agenesis of the corpus callosum and tetralogy of Fallot in some cases. Opitz trigonocephaly and Varadi-Papp syndromes have many common characteristics. - (Source - Diseases Database)

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

Related C Syndrome Info

More information about C Syndrome

  1. C Syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
 

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