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  2. Pregnancy nose is a thing. Here's why it happens - AOL

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  3. Hathaway, whose daughter is now 4, says it took approximately one year after giving birth for the swelling in her nose to reduce. Remember that pregnancy is a big period of emotional and physical ...

  4. Pregnancy nose is a thing. Here's why it happens - AOL

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  5. Nuchal scan - Wikipedia

    en.wikipedia.org/wiki/Nuchal_scan

    A further study reported detection of 88% for trisomy 21 (Down syndrome) and 75% for trisomy 18 (Edwards syndrome), with a 3.3% false-positive rate. [14] Finally, using the additional ultrasound feature of an absent nasal bone can further increase detection rates for Down syndrome to more than 95%.

  6. Noonan syndrome - Wikipedia

    en.wikipedia.org/wiki/Noonan_syndrome

    Noonan syndrome; Other names: Male Turner syndrome, Noonan–Ehmke syndrome, Turner-like syndrome, Ullrich–Noonan syndrome [1] A 12-year-old girl with Noonan syndrome, displaying typical webbed neck and double structural curve with rib deformity. Specialty: Medical genetics, pediatrics: Symptoms

  7. Hemihypertrophy - Wikipedia

    en.wikipedia.org/wiki/Hemihypertrophy

    An 8-year-old Afghani girl with congenital hemihypertrophy of the right arm and hand Full-body hemihypertrophy Hemihypertrophy, now more commonly referred to as hemihyperplasia in the medical literature, is a condition in which one side of the body or a part of one side of the body is larger than the other to an extent considered greater than ...

  8. ‘Two different people’: Woman goes viral after getting ...

    www.aol.com/two-different-people-woman-goes...

    A woman has gone viral on TikTok after sharing her extreme “pregnancy nose”, which has left her completely unrecognisable. Towards the end of her first trimester, Tyreece Wood noticed that the ...

  9. Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Down_syndrome

    Down syndrome or Down's syndrome, [12] also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. [3] It is usually associated with developmental delays, mild to moderate intellectual disability , and characteristic physical features.