Literature DB >> 7173481

Renal--skeletal--ear- and facial-anomalies in combination with the Mayer--Rokitansky--Küster (MRK) syndrome.

W N Willemsen.   

Abstract

The combination of the Mayer--Rokitansky--Küster (MRK) syndrome with renal anomalies is well known (incidence: 36%). The combination with skeletal anomalies is also known (incidence: 10%). However, the coincidence with ear anomalies is rare, and the coincidence with facial anomalies is extremely rare. The combination of the MRK syndrome with renal, skeletal, ear and facial anomalies is described in a case report with a review of the literature. It is not only worthwhile to be alert for urinary tract anomalies in patients with the MRK syndrome, but also to study the skeletal and auditory systems in these patients.

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Year:  1982        PMID: 7173481     DOI: 10.1016/0028-2243(82)90046-6

Source DB:  PubMed          Journal:  Eur J Obstet Gynecol Reprod Biol        ISSN: 0301-2115            Impact factor:   2.435


  5 in total

1.  MURCS association: case report and review.

Authors:  C Braun-Quentin; C Billes; B Böwing; D Kotzot
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

2.  A successful laparoscopic neovaginoplasty using peritoneum in Müllerian agenesis with inguinal ovaries accompanied by primary ovarian insufficiency.

Authors:  Seonghye Gweon; Jisun Lee; Suna Hwang; Kyoung Joo Hwang; Miran Kim
Journal:  Obstet Gynecol Sci       Date:  2016-07-13

3.  Evaluation of radiographic abnormalities of the hand in patients with the Mayer-Rokitansky-Küster-Hauser syndrome.

Authors:  E H Strübbe; C J Thijn; W N Willemsen; R Lappöhn
Journal:  Skeletal Radiol       Date:  1987       Impact factor: 2.199

Review 4.  The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches.

Authors:  Daniel Guerrier; Thomas Mouchel; Laurent Pasquier; Isabelle Pellerin
Journal:  J Negat Results Biomed       Date:  2006-01-27

5.  MURCS (Müllerian duct aplasia-renal agenesis-cervicothoracic somite dysplasia): a rare cause of primary amenorrhoea.

Authors:  Sunil Kumar; Shruti Sharma
Journal:  Oxf Med Case Reports       Date:  2016-04-20
  5 in total

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