What is another word for Congenital Hypocupremia?
Pronunciation: [kənd͡ʒˈɛnɪtə͡l hˌa͡ɪpə͡ʊkʌpɹˈiːmi͡ə] (IPA) 
Congenital Hypocupremia, also known as Menkes disease, is a rare genetic disorder that affects copper metabolism in the body. It leads to a copper deficiency, resulting in various developmental and neurological abnormalities. While "Congenital Hypocupremia" is a commonly used term to describe this condition, it is essential to understand synonymous terms associated with Menkes disease. "Menkes syndrome", "Kinky hair disease", and "Steely hair syndrome" are alternative names used interchangeably to refer to Congenital Hypocupremia. These synonyms highlight the key symptoms of the disease, such as unusual hair texture and color, and provide a clearer understanding of the condition.
