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    Children's Health

    Medical Reference Related to Children's Health

    1. Chromosome 21 Ring

      Important It is possible that the main title of the report Chromosome 21 Ring is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    2. Noonan Syndrome

      Important It is possible that the main title of the report Noonan Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    3. Oculocerebral Syndrome with Hypopigmentation

      Important It is possible that the main title of the report Oculocerebral Syndrome with Hypopigmentation is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    4. Greig Cephalopolysyndactyly Syndrome

      Important It is possible that the main title of the report Greig Cephalopolysyndactyly Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    5. Spondyloepiphyseal Dysplasia, Congenital

      Important It is possible that the main title of the report Spondyloepiphyseal Dysplasia, Congenital is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    6. Sialidosis

      Important It is possible that the main title of the report Sialidosis is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    7. X-Linked Myopathy with Excessive Autophagy

      X-linked myopathy with excessive autophagy (XMEA) is an extremely rare genetic disorder characterized by muscle disease (myopathy). The disorder is fully expressed in males only and is characterized by slowly progressive muscle weakness,especially in the legs. Onset is usually during childhood often between 5-10 years of age. XMEA occurs due to mutations of an unidentified gene on the X ...

    8. May Hegglin Anomaly

      Important It is possible that the main title of the report May Hegglin Anomaly is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    9. Chromosome 6, Partial Trisomy 6q

      Important It is possible that the main title of the report Chromosome 6, Partial Trisomy 6q is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

    10. Rosai-Dorfman Disease

      Important It is possible that the main title of the report Rosai - Dorfman Disease is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. ...

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