Gitelman syndrome
An inherited disorder caused by mutations in the SLC12A3 gene. It is characterized by deficient reabsorption of electrolytes in the distal convoluted tubules of the kidneys. It results in hypochloremic metabolic alkalosis, hypokalemia, hypocalciuria, and hypomagnesemia.
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SANKALPA SUPERSPECIALITY HOSPITAL
M B B S
BANGALORE MEDICAL COLLEGE AND RESEARCH CENTRE
M B B S
LLRM
Senior Resident
Super Specialist in Reproductive Endocrinology
Private Practise
Md
New Phc
Ayush Pharmashist
Kanpur Para Medical Institute
d.pharma
Trending Cases
What is the treatment of ulcer in angle of both lips again and again? I give tess oint there is recover but it produce again what is cause and treatment?
Dr. Nirmal Shah0 Like1 AnswerA female 36 years, gravida 3 para 2 comes with complaints of headache, loss of sight and is in labour with poor cervical dilatation progress. on admission, the BP is 178/102 with no history of convulsions and magnesium sulphate is given. A LSCS is performed under spinal anesthesia with BP stabilised. she is transferred to ICU for post operative management with BP continuing to increase . After 5 days, a feedback is given that the patient is discharged and gained her sight. What caused the loss of sight?
Dr. Prashant Vedwan1 Like0 Answer