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'''SCARF Syndrome''' is an extremely rare [[intersex]] variation that estimated to effect one in a million newborns. It can effect both [[CTM]] and [[CTF]] children alike.
In both CTF and CTM individuals, physical symptoms may include loose skin, a small chin, a drooping eyelid, unaligned eyes, eyefolds, high/broad nasal roots, teeth defects, neck webs, short necks, abnormal chest shapes, [[Secondary Sex Agenesis|small nipples]], a short sternum, umbilical hernia, diastasis recti, abnormal vertebrae, abnormal skulls, turned ears, sparse hair, abnormal nails, and joint flexibility. They are often described as appearing "elderly" due to their physical appearance.<ref>https://en.wikipedia.org/wiki/SCARF_syndrome#Signs_&_Symptoms</ref> Possible complications for those with this variation include dyspnea, heart disorders, joint disorders, and dislocations of multiple joints.<ref>[https://en.wikipedia.org/wiki/SCARF_syndrome#:~:text=SCARF%20syndrome%20is%20a%20rare,with%20Lenz%2DMajewski%20hyperostotic%20dwarfism. https://en.wikipedia.org/wiki/SCARF_syndrome#:~:text=SCARF%20syndrome%20is%20a%20rare,with%20Lenz%2DMajewski%20hyperostotic%20dwarfism.]</ref>
In CTF individuals, [[clitoromegaly]] and [[Ambiguous Genitalia|ambiguous genitalia]] is common. In CTM individuals, [[Agenital|cryptorchidism, micropenises]], clefts in the scrotum, [[hypospadias]], and ambiguous genitalia is common as well.<ref>https://rarediseases.info.nih.gov/diseases/247/scarf-syndrome</ref>
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