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Results 1 - 10 of 84 for Heart defect -tongue hematoma -"poly syndactyly" syndrome
  1. RIT1 gene 
    ... characterized by mildly unusual facial characteristics, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms. People with Noonan syndrome caused by RIT1 gene mutations often have swelling ...
    https://medlineplus.gov/genetics/gene/rit1 - Genetics
  2. Noonan syndrome 
    ... characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.People with Noonan syndrome have distinctive facial features such as a deep ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  3. Jacobsen syndrome 
    ... although affected individuals have lived into adulthood. Complex heart defects are a leading cause of death in people with Jacobsen syndrome. Bleeding episodes and infections can also be life-threatening ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  4. SOS1 gene 
    ... have been identified in the SOS1 gene. Noonan syndrome is characterized by mildly unusual facial characteristics, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and ...
    https://medlineplus.gov/genetics/gene/sos1 - Genetics
  5. RAF1 gene 
    ... have been identified in the RAF1 gene. Noonan syndrome is characterized by mildly unusual facial characteristics, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and ...
    https://medlineplus.gov/genetics/gene/raf1 - Genetics
  6. Noonan Syndrome (For Parents) (Nemours Foundation)  
    ... Lordosis, Pulmonary valvular stenosis, typical face dysmorphology, ... cardiofaciocutaneous syndrome, Costello syndrome, neurofibromatosis type ...
    https://kidshealth.org/en/parents/noonan-syndrome.html - External Health Links
  7. Platelet Disorders (National Library of Medicine)  
    ... to blood vessel walls. This can cause excessive bleeding. There are different types of in von Willebrand Disease; treatment depends on which type you have. NIH: National Heart, Lung, and Blood Institute
    https://medlineplus.gov/plateletdisorders.html - Health Topics
  8. PTPN11 gene 
    ... become cancerous. More than 90 mutations causing Noonan syndrome have been identified in the PTPN11 gene. This condition is characterized by mildly unusual facial characteristics, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  9. Alpha thalassemia 
    ... severe anemia, an enlarged liver and spleen (hepatosplenomegaly), heart ... bleeding.HbH disease causes mild to moderate anemia, hepatosplenomegaly, ...
    https://medlineplus.gov/genetics/condition/alpha-thalassemia - Genetics
  10. Eisenmenger syndrome 
    Surgery as early as possible to correct the heart defect can prevent Eisenmenger syndrome.
    https://medlineplus.gov/ency/article/007317.htm - Medical Encyclopedia
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