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Müllerian anomalies can be part of a multiple malformation syndrome. [1] [3] Studies have estimated that Mullerian anomalies can affect between 4 percent and nearly 7 percent of the female population. [4] [5] Müllerian anomalies occur as a congenital malformation of the Müllerian ducts during embryogenesis.
Congenital Anomalies XV 760–779: Certain Conditions originating in the Perinatal Period XVI 780–799: Symptoms, Signs and Ill-defined Conditions XVII 800–999: Injury and Poisoning E800–E999: Supplementary Classification of External Causes of Injury and Poisoning: V01–V82
Müllerian agenesis, also known as Müllerian aplasia, vaginal agenesis, or Mayer–Rokitansky–Küster–Hauser syndrome (MRKH syndrome), is a congenital malformation characterized by a failure of the Müllerian ducts to develop, resulting in a missing uterus and variable degrees of vaginal hypoplasia of its upper portion.
A mesenteric cyst (MeSH C04.182.473) is a cyst in the mesenterium, and is one of the rarest abdominal tumors, with approximately 822 cases reported since 1507. [1] The incidence is between 1 per 100,000 to 1 per 250,000 hospital admissions. [1] Tillaux's triad named after the French surgeon Paul Jules Tillaux can be
The American Fertility Society (now American Society of Reproductive Medicine) Classification distinguishes: Class I—Müllerian agenesis (absent uterus). This condition is represented by the hypoplasia or the agenesis (total absence) of the different parts of the uterus: Vaginal hypoplasia or agenesis; Cervical hypoplasia or agenesis
Intestinal malrotation is a congenital anomaly of rotation of the midgut.It occurs during the first trimester as the fetal gut undergoes a complex series of growth and development.
Persistent Müllerian duct syndrome (PMDS) is the presence of Müllerian duct derivatives (fallopian tubes, uterus, and/or the upper part of the vagina) [1] in what would be considered a genetically and otherwise physically normal male. [2]
Biliary cystadenoma and cystadenocarcinoma constitute less than 5% of intrahepatic cysts originating from the bile duct. [6] Cystadenomas in liver are often confused with hydatid cyst as their appearance on various imaging techniques is nearly same. [7] Treating cystadenomas as hydatid cyst has resulted in recurrence of the cyst. [7]