Duplication 5pter p13.3 (medical condition): A rare chromosomal disorder characterized by cortico-adrenal hypoplasia, mental retardation, seizures and a blood abnormality.
See also:
Chromosome 5, trisomy 5pter p13 3:
»Introduction: Chromosome 5, trisomy 5pter p13 3
»Symptoms of Chromosome 5, trisomy 5pter p13 3
These medical condition or symptom topics may be relevant to medical information for Duplication 5pter p13.3:
Duplication 5pter p13.3 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Duplication 5pter p13.3, or a subtype of Duplication 5pter p13.3,
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 Duplication 5pter p13.3 as a "rare disease".
Source - Orphanet
Duplication 5pter p13.3: Another name for Chromosome 5, trisomy 5pter p13 3 (or close medical condition association).
»Introduction: Chromosome 5, trisomy 5pter p13 3
»Symptoms of Chromosome 5, trisomy 5pter p13 3
Some of the symptoms of Duplication 5pter p13.3 incude:
Read more about symptoms of Duplication 5pter p13.3 (Chromosome 5, trisomy 5pter p13 3)
Source - NIH
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