My son Nathaniel has POMC he is the ONLY known person in the USA with it.... (there are less than 50 cases known in the world) Pro-opiomelanocortin Deficiency Disorder is Rare, it is considered a 'Rare/Orphan Disease' POMC affects the second chromosome = 2p 23.3 Molecular Location on chromosome 2: base pairs 25,383,721 to 25,391,558 to be exact Not every person that has POMC will or does have all the same issues. BUT This is what Nathaniel deals with because of POMC = extended linear growth and congenital hyperphagia (insatiable hunger)~a life threatening issue and congenital secondary adrenal insufficiency ~considered rare~another life threatening issue and congenital hypothyroidism~considered rare~ and yet another life threatening issue and congenital hyopituitaryisum~considered the 'brain' of all endocrine glands and congenital hypothalamus disorder~he is unable to control his body temperature~an yes, another life threatening issue and Early...
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