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Neuroectodermal melanolysosomal disease (medical condition): A rare congenital syndrome characterized excessive fetal growth, skull abnormalities, extra fingers or toes and other abnormalities.
See also:
Elejalde syndrome:
»Introduction: Elejalde syndrome
»Symptoms of Elejalde syndrome
These medical condition or symptom topics may be relevant to medical information for Neuroectodermal melanolysosomal disease:
Neuroectodermal melanolysosomal disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Neuroectodermal melanolysosomal disease, or a subtype of Neuroectodermal melanolysosomal disease,
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 melanolysosomal disease as a "rare disease".
Source - Orphanet
Neuroectodermal melanolysosomal disease: Another name for Elejalde syndrome (or close medical condition association).
»Introduction: Elejalde syndrome
»Symptoms of Elejalde syndrome
Some of the symptoms of Neuroectodermal melanolysosomal disease incude:
See full list of 10 symptoms of Neuroectodermal melanolysosomal disease (Elejalde syndrome)
Source: Diseases Database
Source - NIH
Source: Diseases Database
Search to find out more about Neuroectodermal melanolysosomal disease:
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