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'''SERKAL Syndrome''' is an [[intersex]] condition 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 condition have growth delay, oligohydramnios, a small lung, an absent kidney, abnormalities in the nostrils
30%-79% of those witth this condition 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]], 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.
== Causes ==
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