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Genetics  (Expert Forum)
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undiagnosed benign congenital hypotonia
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Welcome to the Genetics Forum! Questions in the Genetics Forum are being answered by genetic experts from AccessDNA. This forum is for questions and support regarding a person’s predisposition to a variety of medical conditions such as Ashkenazi Jewish Diseases, Bleeding Disorders, Blood Clotting Disorders, Cancer Genetics and Hereditary Cancer Syndromes, Chromosome Abnormalities, Congenital Birth Defects, Cystic Fibrosis, Family History, Fragile X Syndrome, Infertility, Newborn Screening, Rare Genetic Disorders, Prenatal Screening and Testing. This forum is for questions and support regarding a person’s predisposition to a variety of medical conditions such as Alzheimer’s Disease, Blood-clotting Disorders, Breast Cancer, Cystic Fibrosis, Diabetes, Marfan Syndrome, Ehlers-Danlos Syndrome, etc.

undiagnosed benign congenital hypotonia

by ash0301, Sep 12, 2009 09:18AM
My daught. just turned a year old, she is a pure joy. However, she is a big mystery to me and her father, as well as to all of doctors. I knew somthing was wrong immediatly after she was born. I was assured she was fine. She was extremly quiet and laid back. Didn't make a sound after she was born, a happy baby. When we brought her home from the hosp I noticed that she had no stepping reflex, she couldn't bare any weight on her legs. She was diagnosed with Benign congenital hypotonia around 3 m. She has microcephaly. (16 is her head circ. right now and shes a year old, 29 inches long, and 18 lbs 9 oz), dev delay (performes on a 4-5 month level), upper GI problems, hx of resp. issues, has a lot of mucus build up has a very hard time manageing and coughing up (coughing fits in which she turns blue before she's finally able to cough phlegm up - these fits are usually very violent. She cannot hold a bottle, sit up, crawl, walk. She was able to roll both ways around 10 m., once u get her verticle there is just nothing there. She sees a ped. Neuro., GI specialist, ped pulmon., PT, OT, ST and will be having a PEG placed soon. She has had many tests - Gen. workup just recently came back normal. Cpk tests were 370 and I was informed that it was a little high but still normal, her cystic fibrosis test was normal, mri and eeg normal. An endoscopic proc. performed after she spit up blood found the beginnings of an ulceration in her stomach. Biopsies of stomach and esophagus were normal. She was put on carofate and prevacid but was hospitalized again when she couldn't keep her meds down and her condition got worse. They inserted a NG tube. I think she should have a muscle biopsy but the drs havent pushed for it.She has been fitted with AFOs, a stander and a bath seat. Her reflexes are good. She had rsv at 1 m in which she was hosp for 3 days, and the flu at 6 m. with hosp. as well. Thank u so very much for ur time.

by Jordanna Joaquina, MS, CGC, Sep 15, 2009 03:56PM
To: ash
We recommend that your daughter meet with a medical geneticist for evaluation. A medical (clinical) geneticist is a doctor who specializes in genetic disorders. A medical geneticist will perform a physical exam as well as review all your daughter's test results, your pregnancy history and the family history.

A clinical geneticist looks for signs and symptoms that may be caused by an underlying genetic syndrome. You can find a medical geneticist in your area at the American College of Medical Genetics website.

We wish your family the best.
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