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Neuroectodermal syndrome, Zunich type (medical condition): A very rare genetic syndrome characterized by a range of symptoms such as colobomas of the eye, heart defects, ichthyosiform dermatosis, mental retardation and ear defects.
See also:
Zunich neuroectodermal syndrome:
»Introduction: Zunich neuroectodermal syndrome
»Symptoms of Zunich neuroectodermal syndrome
These medical condition or symptom topics may be relevant to medical information for Neuroectodermal syndrome, Zunich type:
Neuroectodermal syndrome, Zunich type is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Neuroectodermal syndrome, Zunich type, or a subtype of Neuroectodermal syndrome, Zunich type,
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 if affects 1 person per 2,000.
They list Neuroectodermal syndrome, Zunich type as a "rare disease".
Source - Orphanet
Neuroectodermal syndrome, Zunich type: Another name for Zunich neuroectodermal syndrome (or close medical condition association).
»Introduction: Zunich neuroectodermal syndrome
»Symptoms of Zunich neuroectodermal syndrome
Some of the symptoms of Neuroectodermal syndrome, Zunich type incude:
Source - NIH
Search to find out more about Neuroectodermal syndrome, Zunich type:
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