Refine your search
Collections
Co-Authors
Journals
Year
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Mittal, Aniket
- Mayer-Rokitansky-Kuster-Hauser Syndrome A Case Report
Abstract Views :220 |
PDF Views:0
Authors
Affiliations
1 Department of Medicine, Pt. B.D. Sharma University of Health Sciences, Rohtak-124001 (Haryana), IN
2 Department of Medicine, Mahadevappa Rampure Medical College, Gulbarga, Karnataka, IN
3 Department of pathology, Pt. B.D. Sharma University of Health Sciences, Rohtak-124001 (Haryana), IN
1 Department of Medicine, Pt. B.D. Sharma University of Health Sciences, Rohtak-124001 (Haryana), IN
2 Department of Medicine, Mahadevappa Rampure Medical College, Gulbarga, Karnataka, IN
3 Department of pathology, Pt. B.D. Sharma University of Health Sciences, Rohtak-124001 (Haryana), IN
Source
The Indian Practitioner, Vol 71, No 3 (2018), Pagination: 39-42Abstract
Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) is a form of Mullerian agenesis and is a cause of primary amenorrhea in females. It is characterized by congenital aplasia of uterus and upper two third of vagina showing normal development of secondary sexual characters and normal 46XX karyotype. Here we describe a case of a young female presenting with primary amenorrhea that was diagnosed as a case of Type 2 MRKH syndrome.Keywords
Mayer-Rokitansky-Kuster-Hauser Syndrome, Mullerian Agenesis, Primary Amenorrhea, Aplasia Of Uterus.
References
- Strubbe EH, Cremers CWRJ, Willemsen WNP, Rolland R, Thijn CJ. The Mayer - Rokitansky Kuster - Hauser (MRKH) syndrome without and with associated features: two separate entities? Clin Dysmorphol. 1994;3:192–199.
- Duncan PA, Shapiro LR, Stangel JJ, Klein RM, Addonzizio JC. The MURCS association: Müllerian duct aplasia, renal aplasia and cervicothoracic somite dysplasia. J Pediatr. 1979;95(3):399–402.
- Morcel K, Camborieux L. Mayer-RokitanskyKuster-Hauser (MRKH) syndrome. Orphanet J Rare Dis. 2007;2:13.
- Strubbe EH, Willemsen WN, Lemmens JA, Thijn CJ, Rolland R. Mayer-Rokitansky-Kuster-Hauser syndrome: distinction between two forms based on excretory urographic, sonographic and laparoscopic findings. Am J Roentgenol. 1993;160(2):331–334.
- Cremers CW, Strubbe EH, Willemsen WN. Stapedial ankylosis in the Mayer-RokitanskyKuster-Hauser syndrome. Arch Otolaryngol Head Neck Surg. 1995;121:800–803.
- Wellesley DG, Slaney SF. MURCS in a male? Med Genet 1995;32:314-315.
- Pavanello R de CM, Eiger A, Otto PA. Relationship between Mayer-Rokitansky-Kuster (MRK) anomaly and hereditary renal adysplasia (HRA). Am Med Genet 1998;29:845-9.
- Burel A, Mouchel T, Odent S et al. Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina). J Negat Results Biomed. 2006;5:4.
- Biason-Lauber A, Konrad D, Navratil F, Schoenle EJ. A WNT4 mutation associated with Mullerianduct regression and virilization in a 46 XX woman. N Engl J Med. 2004;351:792–798.
- Bendavid C, Pasquier L, Watrin T et al. Phenotypic variability of a 4q34--qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother. Eur J Med Genet. 2007;50:66–72.
- Sharma BB, Sharma S, Singh Y, Balesa J. MayerRokitansky-Kuster-Hauser Type I Syndrome– A Case Report. Indian J Case Reports. 2015;1(1):8-10.