Odontogenic keratocyst and uterus bicornis in nevoid basal cell carcinoma syndrome: Case report and literature review [PDF]
, 2006 Nevoid basal cell carcinoma syndrome (NBCCS), an autosomal dominant disorder with a high degree of penetrance and variable expressivity, is characterized by basal cell carcinomas, odontogenic keratocysts, palmar and/or plantar pits and ectopic ...
F. MORGESE +3 more
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Wnt5a Regulates Embryonic Müllerian Duct Development Through the Non-Canonical Wnt PCP Pathway
CellsMüllerian anomalies are anatomical variations of the female reproductive tract resulting from the incomplete development of the embryonic Müllerian ducts.
Isaac Kyei-Barffour +3 more
doaj +1 more source
Imaging the developing human external and internal urogenital organs with light sheet fluorescence microscopy. [PDF]
, 2020 Technological advances in three-dimensional (3D) reconstruction techniques have previously enabled paradigm shifts in our understanding of human embryonic and fetal development. Light sheet fluorescence microscopy (LSFM) is a recently-developed technique
Baskin, Laurence +9 more
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Laparoscopic removal of mullerian duct remnants in boys [PDF]
, 2004 : Purpose: Mullerian duct remnants (MDRs) are present in a male pseudohermaphroditic form characterized by failure of the mullerian duct to regress due to insufficient production or peripheral action of mullerian inhibiting substance.
Aquino, A. +6 more
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Mini review: Asymmetric Müllerian duct development in the chicken embryo
Frontiers in Cell and Developmental BiologyMüllerian ducts are paired embryonic tubes that give rise to the female reproductive tract. In humans, the Müllerian ducts differentiate into the Fallopian tubes, uterus and upper portion of the vagina.
Juan L. Tan +2 more
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Congenital scoliosis associated with agenesis of the uterine cervix. Case report
BMC Women's Health, 2004 Background Alterations in the normal sequence of development of müllerian ducts lead to a wide spectrum of reproductive tract abnormalities. A rare form of lack of development, regarding a short tract of the müllerian ducts, leads to the isolated ...
Monica Matteo +2 more
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Persistent Mullerian Duct Syndrome
Annals of Pathology and Laboratory Medicine, 2019 Persistent Mullerian duct syndrome (PMDS) is usually an accidental finding either during orchidopexy or during routine inguinal hernia repair in male patients presenting with undescended testes. It is a rare form of internal male pseudohermaphroditism caused by defect in synthesis or action of Mullerian inhibiting factor due to which Mullerian ...
Shabnam Izhar +2 more
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Role of imaging in the diagnosis and management of complete androgen insensitivity syndrome in adults [PDF]
, 2013 Complete androgen insensitivity syndrome is an X-linked recessive androgen receptor disorder characterized by a female phenotype with an XY karyotype.
De Visschere, Pieter +4 more
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Bicervical Normal Uterus with Normal Vagina and Anteroposterior Disposition of the Double Cervix
Case Reports in Medicine, 2011 We report a very uncommon uterine anomaly consisting on a normal uterus, a double cervix with an anteroposterior disposition, and absence of vaginal septum. A 36-years-old woman with one child and absence of past reproductive disorders was examined for a
José Morales-Roselló +1 more
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Twin Pregnancy in a Woman with Uterus Didelphys [PDF]
, 2011 Uterus didelphys is one of the congenital uterine anomalies due to defective medial fusion of mullerian ducts. This anomaly is known to have poor reproductive outcome and women with this condition often have to be treated for infertility.
Bhattacharya, Sohini +1 more
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