CAM topics in Medical Genetics mb021302dr

Genetic defects leading to malabsorption in the intestine

Malabsortion of lysine, ornithine and cystine

Genetic defects leading renal malabsortion

Cystinuria in renal carrier protein defects

Genetic disorders of amino acid transport

Hartnup disease and inability to transport neutral amino acids

Nutritional dependency versus deficiency

Cardiovascular system

Apolipoprotein in cardiovascular disease & dietary recommendations

Vitamin E and congenital heart disease

Garlic and congenital hypercholesteremia

 

Nervous system

Pyridoxin dependency and neurological malfunction

Genetic factors in hypoglycemic behaviors & dietary palliative measures

Headache due to allergic hyperhistaminia and nutritional palliation [ B6, C, Panthothenic acid]

Magnesium and epilespy

Vitamin E and dementia

Muscular system

Myastenia gravis and acetylcholin synthesis [ B1, B2, B5, B6, K, Cholin]

Muscle weakness, congenital adrenal exhaustion and panthothenic acid

Muscle spasms, multiple sclerosis and magnesium

 

Genetics effects of microwave exposure

i.e. reproductive cell damage

 

Genetics effects of ultra-low frequency exposure

i.e. embryonic malformations

 

Genetic considerations in embryonic development of the acupuncture meridian system (possibly)

 

Genetic predisposition to verterbral subluxation / osteopathic lesion (possibly)