Galactosemia
An autosomal recessive inherited metabolic disorder caused by mutations in the GALE, GALK1, and GALT genes. It is characterized by deficiency of the enzymes responsible for the metabolism of galactose. Signs and symptoms include intellectual disability, hepatomegaly, hepatic failure, and renal failure.
So first type is stress induced amenorrhea, second is PCOS,third is ovarian failure and fourth is prolactin induced amenorrhea.
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Prolonged conjugated hyperbilirubinemia in a neonate is termed as neonatal cholestasis
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Recent Cases of Galactosemia
Browse recently discussed Galactosemia cases by specialistsTop Cases of Galactosemia
Selected by editors, top cases are known for unique problem or best solutionTop Galactosemia Doctors on Curofy
Top doctors who continously share their opinions on GalactosemiaNational Institute of Medical Science
Md Paediatrics
National Institute of Medical Science
MD pediatrics
Self Emploid(private Clinic)
Morbi
Shri M P Shah Medical College Jamnagar
M B B S
Super Specialist in Reproductive Endocrinology
Sanjay Gandhi Postgraduate Institute of Medical Sciences
Senior Resident
Sanjay Gandhi Postgraduate Institute of Medical Sciences
PDCC Paediatric Gastroenterology & Hepatology
Private Practise
Md
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Paratesticular tumours are masses of slow & indolent growth & in most cases of benign nature, in these cases the treatment of choice is simple extirpation of the lesion. A paratesticular mass may derive from a number of structures that surround the testis within the scrotum; most commonly, they derive from the spermatic cord. Dr. Vivek Jha is sharing a clinical case of "Large Paratesticular Growth" managed with surgical expertise by him. Share your views on the case & learn new things.
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Check how quickly can you solve these questions using your clinical knowledge. Solve & get a chance to be the top performer. We are Live Now.
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Check out the answer for Quick Brains quiz.
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