[A case of pseudo-Bartter's syndrome associated with hypokalemic myopathy]. 1988

T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
Gifu Prefectural Gero Hot Spring Hospital and Medical Institute.

A case of pseudo-Bartter's syndrome associated with hypokalemic myopathy was presented. A 37-year-old housewife was admitted to our hospital because of muscle cramps with muscle weakness and tetany. There was a history of facial edema and constipation, which have been managed with "Kanpo medicine (Chinese medicine)" and laxatives for several years. The patient was amenorrhea 3 months before entry. She began to experience muscle weakness and muscle cramps associated with gait disturbance 2 or 3 months before admission. On physical examination, she was thin with positive Trousseau's and Chvostek's signs. Laboratory studies revealed hypokalemia, low urinary excretion of potassium, hypocalcemia, metabolic alkalosis, elevated creatine phosphokinase (CPK), increased levels of plasma renin activity and plasma aldosterone concentration, and decreased sensitivity to pressor effect of angiotensin II. Potassium supplementation resulted in restoration of her symptoms and normalization of low serum calcium and elevated CPK levels. She was diagnosed to be pseudo-Bartter's syndrome due to anorexia nervosa. The mechanism(s) of hypokalemia in our case was discussed.

UI MeSH Term Description Entries
D007008 Hypokalemia Abnormally low potassium concentration in the blood. It may result from potassium loss by renal secretion or by the gastrointestinal route, as by vomiting or diarrhea. It may be manifested clinically by neuromuscular disorders ranging from weakness to paralysis, by electrocardiographic abnormalities (depression of the T wave and elevation of the U wave), by renal disease, and by gastrointestinal disorders. (Dorland, 27th ed) Hypopotassemia,Hypokalemias,Hypopotassemias
D009135 Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. Muscle Disorders,Myopathies,Myopathic Conditions,Muscle Disorder,Muscular Disease,Myopathic Condition,Myopathy
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006929 Hyperaldosteronism A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA. Aldosteronism,Conn Syndrome,Conn's Syndrome,Primary Hyperaldosteronism,Conns Syndrome,Hyperaldosteronism, Primary,Syndrome, Conn,Syndrome, Conn's
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D001477 Bartter Syndrome A group of disorders caused by defective salt reabsorption in the ascending LOOP OF HENLE. It is characterized by severe salt-wasting, HYPOKALEMIA; HYPERCALCIURIA; metabolic ALKALOSIS, and hyper-reninemic HYPERALDOSTERONISM without HYPERTENSION. There are several subtypes including ones due to mutations in the renal specific SODIUM-POTASSIUM-CHLORIDE SYMPORTERS. Aldosteronism with Hyperplasia of the Adrenal Cortex,Bartter Disease,Bartter's Disease,Bartter's Syndrome,Juxtaglomerular Hyperplasia with Secondary Aldosteronism,Bartters Disease,Bartters Syndrome,Syndrome, Bartter,Syndrome, Bartter's

Related Publications

T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
August 1997, The Journal of rheumatology,
T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
February 1983, Klinische Wochenschrift,
T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
May 1987, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine,
T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
October 2000, Nihon Jinzo Gakkai shi,
T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
December 1984, Endocrinologia japonica,
T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
February 1985, Casopis lekaru ceskych,
T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
August 2005, Pediatric nephrology (Berlin, Germany),
T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
August 2003, Casopis lekaru ceskych,
T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
July 1972, Das Deutsche Gesundheitswesen,
T Imai, and M Izai, and S Narimiya, and M Nagaki, and T Adachi, and T Oohira, and K Kamikubo, and M Shiooka, and H Fujioka, and Y Kotoo
May 1984, Journal of the Royal Society of Medicine,
Copied contents to your clipboard!