What is baby franklins disability?
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Answer:
Franklin has been diagnosed with Wiedemann Steiner Syndrome
Wiedemann Steiner Syndrome
Wiedemann–Steiner syndrome (WSS) is a rare genetic disorder that causes developmental delay, unusual facial features, short stature, and reduction in muscle tone (hypotonia). The syndrome was originally described in 1989 by Hans-Rudolf Wiedemann. The genetic basis for the syndrome was identified by Dr.
https://en.wikipedia.org › wiki
Wiedemann–Steiner syndrome - Wikipedia
. Wiedemann Steiner Syndrome is a rare genetic disorder resulting from mutations. and the MLL gene on the long arm of chromosome 11.
Wiedemann Steiner Syndrome
Wiedemann–Steiner syndrome (WSS) is a rare genetic disorder that causes developmental delay, unusual facial features, short stature, and reduction in muscle tone (hypotonia). The syndrome was originally described in 1989 by Hans-Rudolf Wiedemann. The genetic basis for the syndrome was identified by Dr.
https://en.wikipedia.org › wiki
Wiedemann–Steiner syndrome - Wikipedia
. Wiedemann Steiner Syndrome is a rare genetic disorder resulting from mutations. and the MLL gene on the long arm of chromosome 11.
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