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This syndrome can cause a [[Agenital|missing or undescended testicle, a micropenis]], and/or [[hypospadias]] in [[CTM]]/[[AMAB]] individuals. CTF/AFAB individuals with this syndrome tend to have labial hypoplasia (one or both labia missing.)
This syndrome often comes with [[Secondary Sex Agenesis|low muscle tone]], strabismus, hearing loss, undersized kidneys, foot abnormalities, scoliosis, rib-cage abnormalities, umbilical and inguinal hernias, and brain defects that often lead one to fall on the [[Neurodivergent|autism spectrum.]] Some of these symptoms may classify one with this syndrome as physically [[disabled]].<ref>{{Archive|Site=web|URL=https://rarediseases.org/rare-diseases/chromosome-18-ring/}}</ref>
== Causes ==
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== History ==
This syndrome was first reported in 1964.<ref>https://en.wikipedia.org/wiki/Ring_chromosome_18</ref>
== References ==
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