Fanconi syndrome / Proximal ( Type 2 ) Renal Tubular Acidosis -
HTML-код
- Опубликовано: 7 сен 2024
- 📌 𝐅𝐨𝐥𝐥𝐨𝐰 𝐨𝐧 𝐈𝐧𝐬𝐭𝐚𝐠𝐫𝐚𝐦:- / drgbhanuprakash
📌𝗝𝗼𝗶𝗻 𝗢𝘂𝗿 𝗧𝗲𝗹𝗲𝗴𝗿𝗮𝗺 𝗖𝗵𝗮𝗻𝗻𝗲𝗹 𝗛𝗲𝗿𝗲:- t.me/bhanuprak...
📌𝗦𝘂𝗯𝘀𝗰𝗿𝗶𝗯𝗲 𝗧𝗼 𝗠𝘆 𝗠𝗮𝗶𝗹𝗶𝗻𝗴 𝗟𝗶𝘀𝘁:- linktr.ee/DrGB...
Fanconi syndrome / Proximal ( Type 2 ) Renal Tubular Acidosis - Pathology
Fanconi syndrome is a rare disorder characterized by the wasting of variable amounts of phosphate, glucose, amino acids, and bicarbonate by the proximal renal tubule.
The defect is associated with reduced ATP and Na+/K+ ATPase activity.
Causes of Fanconi syndrome include:
• Inborn errors of metabolism: cystinosis, galactosemia, fructose, tyrosinemia (the most common cause overall is cystinosis)
• X-linked syndromes: Lowe syndrome, Dent’s disease
• Metals: Wilson’s disease, heavy metal toxicity
• Medications: chemotherapy, immunosuppressants, gentamicin, tenofovir, expired tetracyclines
Signs and symptoms of acquired Fanconi syndrome that commonly prompt patients to seek care include:
• Polyuria - caused by loss of excessive amounts of solutes in the urine
• Polydipsia - caused by loss of excessive amounts of solutes in the urine
• Dehydration - caused by loss of excessive amounts of solutes in the urine
• Bone deformities - caused by urinary losses of calcium and phosphate
• Impaired growth - caused by disturbances in mineral and vitamin D metabolism
Rickets and osteomalacia may result from urinary loss of calcium.
The most striking physical exam finding associated with Fanconi syndrome is failure to thrive.
The diagnosis of Fanconi syndrome is made by detecting elevated levels of glucose, amino acids, and electrolytes in the urine.
Serum findings include:
• Hypokalemia
• Hypophosphatemia
• Metabolic acidosis
The treatment of Fanconi syndrome includes replacement of lost electrolytes and bicarbonate to correct the metabolic acidosis.
#fanconisyndrome #fanconisyndromepathology #fanconisyndromeusmle #fanconisyndromeRTA #renaltubularacidosis #type2renaltubularacidosis #renaltubularacidosisfanconisyndrome #renalpathology #nephrology #pathology #neetpg #usmle #usmlestep1 #uworld #mbbs #nationalexittest #nationalexitexam #fanconi #fanconisyndromecauses #fanconisyndromeclinicalfeatures #fanconisyndromediagnosis #fanconisyndrometreatment
Sir i have been following you since first year and still now in my 4th year ....a great job sir
🤝🤝🤝
Allsalla alikum
Doctor your explanation is amazing
Thanks from iraq
TYSM
Its amazing helps alot
Sir, Your lectures are AMAZING, thank You!
Thanknu
@@doctorbhanuprakash Very popular explanation. We want the rest of GUS diseases to be explained by this wonderful doctor. I have sent many messages in some videos and WhatsApp, but no one responds. We hope that they are available.
@@doctorbhanuprakash
Sir, my son having this issue so Fanconi Syndrome , i want to know about the treatment and how long it required treatment.
excellent.Sir please make a video on different seizure disorders and their treatment
suree
Great work Sir 👍
Many thanks
Nice
Sir please make animated video on lateral wall of nose..
I have it will upload soon....
@@doctorbhanuprakash thank u sir😊
Thank you sir,plz can you explane about rta in hindi,its causes,treatment,precautions
Sir in fanconi syndrome, there is alkalinity in urine which promotes calcium stones . Then in bartters syndrome, why there is calcium stones although there is H+ ion secretion in the collecting duct, why there is calcium stone formation in acidic urine?
Doctor in renal tubular acidosis
urine in type 2 is acidic urine and in type 1 is alkaline urine
Is this right
Nicely explained
Tysm ji
Thank you sir,actually my 8 yes child is suffering from rta 2,plz give any important advice to me,plz plz plz sir,
😊😊😊
Dr my son fanconi syndrome problem pls tell me medicine .age 2yr weight 5.5
Sir i want to buy your animated lecture how i can buy
Contact +919885588972 ( whatsapp )