Mrkh syndrome
A rare syndrome of unknown cause that occurs in females. It is characterized by underdeveloped or absent vagina and uterus in an otherwise phenotypically normal female with a normal 46,XX karyotype. Other abnormalities include unilateral renal agenesis, skeletal abnormalities, hearing loss, and heart defects.
Disease Alternative Name
Recent Cases of Mrkh syndrome
Browse recently discussed Mrkh syndrome cases by specialistsCauses of Primary Amennorhea
Top Cases of Mrkh syndrome
Selected by editors, top cases are known for unique problem or best solution4 Views
, 3 Likes
, 5 Answers
Top Mrkh syndrome Doctors on Curofy
Top doctors who continously share their opinions on Mrkh syndromeGandhi Medical College.
M.B.B.S.

Central Hosp Singrauli Mp
Gynec
DGO

Medical Component OfHCM
Remained Incharge Medical Officer with Hon'Ble C.M of J and K for More Than 20 Years from Jan 2000 To October 2020
Govt. Medical College, Jammu
M.S (General Surgery )

Goa Medical College and Hospital
Senior Resident
Goa Medical College , Bambolim Goa
MS OBSTETRICS AND GYNAECOLOGY

Super Specialist in Reproductive Endocrinology

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
27 Views
, 1 Like
, 1 Answer