[[File:Serkal syndrome flag.jpg|thumb|The SERKAL Syndrome flag.]]
'''SERKAL Syndrome''' is an [[intersex]] conditionvariation similar to [[De La Chapelle Syndrome|de la chapelle syndrome]] in which an individual has female chromosomes (XX) however they have a male appearance outwardly. This occurs in 1 in 1,000,000 [[CTM]] individuals.
100% of those with this conditionvariation have growth delay, oligohydramnios, a small lung, an absent kidney, abnormalities in the nostrils, and seizures.
30%-79% of those witth this conditionvariation have abnormalities in the adrenal glands, a cleft in the mouth, ventricular septal defect, pulmonic stenosis, malrotation of the small bowel, an underdeveloped bladder, congenital diaphragmatic hernia, and genital abnormalities (such as having [[Agenital|cryptorchidism, a micropenis]], [[hypospadias]], and/or [[Penoscrotal Transposition|penoscrotal transposition]].)
Other symptoms include having [[Ovotesticular|ovotestes]], low-set ears, a cleft palate, and abnormal restriction within weight and growth as an infant. It is unknown how frequent these symptoms are.
It is important to note that not all the symptoms listed in this page are guaranteed to occur in someone with this conditionvariation, as someone may only experience one or several of these symptoms, yet still hold the conditionvariation.
== Causes ==
This conditionvariation is due to mutation in the ''Wnt4'' gene, which causes sex reversal that occurs during fetal development, in which gonad differentiation occurs. This means they were originally going to develop as female, however only the chromosomes did such, and the rest of the body developed in a male-like fashion.
== Flag ==
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