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2016 ; 42
(6
): 1237-1243
Nephropedia Template TP
gab.com Text
Twit Text FOAVip
Twit Text #
English Wikipedia
Persistent Mullerian Duct Syndrome: a rare entity with a rare presentation in
need of multidisciplinary management
#MMPMID27532119
Da Aw L
; Zain MM
; Esteves SC
; Humaidan P
Int Braz J Urol
2016[Nov]; 42
(6
): 1237-1243
PMID27532119
show ga
A typical male looking adolescent with a legal female gender assignment presented
with haematuria. Investigations led to the diagnosis of Persistent Mullerian Duct
Syndrome. The condition is indeed a rare entity that needs a multidisciplinar
team management. Case hypothesis: A case of Persistent Mullerian Duct Syndrome
undiagnosed at birth because karyotyping was defaulted, thus resulting in a
significant impact on the legal gender assignment and psychosocial aspects.
Promising future implications: The reporting of this case is important to create
awareness due to its rarity coupled with the rare presentation with hematuria as
a possible masquerade to menstruation. There were not only medical implications,
but also psychosocial and legal connotations requiring a holistic
multidisciplinary management.
|Abdomen/diagnostic imaging
[MESH]
|Adolescent
[MESH]
|Disorder of Sex Development, 46,XY/*diagnosis/diagnostic imaging
[MESH]
|Disorders of Sex Development/*diagnosis/diagnostic imaging
[MESH]