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    Aarskog-Scott Syndrome: Difference between revisions

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    30-79% of those with this syndrome have a broad forehead, low set/rotated ears, external ear malformation, a wide nasal bridge, an upturned nasal tip, a long philtrum, a drooping upper eyelid, downslanting eyelids, cognitive impairment, and/or hyperelastic skin.
    30-79% of those with this syndrome have a broad forehead, low set/rotated ears, external ear malformation, a wide nasal bridge, an upturned nasal tip, a long philtrum, a drooping upper eyelid, downslanting eyelids, cognitive impairment, and/or hyperelastic skin.


    5-29% of those with this syndrome have abnormal vertebral segmentation and fusion, [[Neurodivergent|ADHD]], a cleft palate, a cleft lip, epicanthus, cross eyes, an enlarged cornea, delayed teeth growth, jaw abnormalities, a round face, a short neck, a funnel chest, cardiac failure, a back knee, and/or flat feet.
    5-29% of those with this syndrome have abnormal vertebral segmentation and fusion, [[Neurodivergent|ADHD]], a cleft palate, a cleft lip, epicanthus, cross eyes, an enlarged cornea, delayed teeth growth, jaw abnormalities, a round face, a short neck, a funnel chest, cardiac failure, a back knee, and/or flat feet.


    Those with this syndrome may or may not experience a delayed puberty or symptoms that are similar but not quite the same as the ones listed above. Some of the symptoms may classify one with this syndrome as physically [[disabled]].
    Those with this syndrome may or may not experience a delayed puberty or symptoms that are similar but not quite the same as the ones listed above. Some of the symptoms may classify one with this syndrome as physically [[disabled]].
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