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Clinical features of Mayer–Rokitansky–Küster–Haüser syndrome diagnosed at under 16 years old: result...

Clinical features of Mayer–Rokitansky–Küster–Haüser syndrome diagnosed at under 16 years old: result...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2707611718

Clinical features of Mayer–Rokitansky–Küster–Haüser syndrome diagnosed at under 16 years old: results from a questionnaire survey conducted on all institutions of pediatric surgery and pediatric urology in Japan

About this item

Full title

Clinical features of Mayer–Rokitansky–Küster–Haüser syndrome diagnosed at under 16 years old: results from a questionnaire survey conducted on all institutions of pediatric surgery and pediatric urology in Japan

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

Journal title

Pediatric surgery international, 2022-11, Vol.38 (11), p.1585-1589

Language

English

Formats

Publication information

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

More information

Scope and Contents

Contents

Purpose
Mayer–Rokitansky–Küster–Häuser syndrome (MRKH) usually presents with primary amenorrhea after puberty. The present study clarified the clinical features of MRKH diagnosed at under 16 years old.
Methods
We conducted a questionnaire survey to determine the status of MRKH in Japan. Twenty-one MRKH patients were enrolled, and the patie...

Alternative Titles

Full title

Clinical features of Mayer–Rokitansky–Küster–Haüser syndrome diagnosed at under 16 years old: results from a questionnaire survey conducted on all institutions of pediatric surgery and pediatric urology in Japan

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2707611718

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2707611718

Other Identifiers

ISSN

0179-0358

E-ISSN

1437-9813

DOI

10.1007/s00383-022-05201-3

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