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Re: new member Texas

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I would also be interested to know of any other members from Texas.

We live in San and my daughter is SGA but not diagnosed with

RSS. I hope to make a trip to either NY or Chicago this summer to

confirm if she is RSS or not, but we cannot affort 3-month followups

to see Dr H if she is, therefore would like to know if any other

doctors in Texas who is knowledgeable about RSS. My daughters doctors

are from UT Health Science center, her endocronologist is good,

positive, we like him, but is pretty young and has not had much

experience with RSS. But on the plus side he is open minded and

willing to do research and really wants to diagnose her, and has

said he thinks she is candidate for GH therapy, even though he

thinks she is not growth hormone deficient. There was doubt earlier

on whether her short stature was caused by skeletal dysplasia (then

GH would not work) which has now been ruled out.

Sabina mother of Naomi

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