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Results 1 - 10 of 29 for Grange syndrome
  1. Grange syndrome 
    Grange syndrome is a rare condition that primarily affects the blood vessels. It is characterized by narrowing (stenosis) or blockage (occlusion) of arteries ...
    https://medlineplus.gov/genetics/condition/grange-syndrome - Genetics
  2. YY1AP1 gene 
    ... YY1AP1 gene have been identified in people with Grange syndrome. This rare condition causes narrowing (stenosis) and blockage ( ... and tissues, including the kidneys, brain, and heart. Grange syndrome can also be associated with short fingers and ...
    https://medlineplus.gov/genetics/gene/yy1ap1 - Genetics
  3. Vascular Diseases (National Library of Medicine)  
    What are vascular diseases? Your vascular system is your body's network of blood vessels. It includes your: Arteries, which carry oxygen-rich blood from ...
    https://medlineplus.gov/vasculardiseases.html - Health Topics
  4. Cantú syndrome 
    ... 23.0.co;2-l. Citation on PubMed Grange DK, Lorch SM, Cole PL, Singh GK. Cantu syndrome in a woman and her two daughters: Further ... Citation on PubMed van Bon BW, Gilissen C, Grange DK, ... de Vries BB, Hoischen A. Cantu syndrome is caused by mutations in ABCC9. Am J ...
    https://medlineplus.gov/genetics/condition/cantu-syndrome - Genetics
  5. Bohring-Opitz syndrome 
    ... 38686. Citation on PubMed Bohring A, Oudesluijs GG, Grange DK, Zampino G, Thierry P. New cases of Bohring-Opitz syndrome, update, and critical review of the literature. Am ...
    https://medlineplus.gov/genetics/condition/bohring-opitz-syndrome - Genetics
  6. ASXL1 gene 
    ... article on PubMed Central Bohring A, Oudesluijs GG, Grange DK, Zampino G, Thierry P. New cases of Bohring-Opitz syndrome, update, and critical review of the literature. Am ...
    https://medlineplus.gov/genetics/gene/asxl1 - Genetics
  7. Myhre syndrome 
    ... or Free article on PubMed Central Starr LJ, Grange DK, Delaney JW, Yetman AT, Hammel JM, Sanmann JN, Perry DA, Schaefer GB, Olney AH. Myhre syndrome: Clinical features and restrictive cardiopulmonary complications. Am J ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics
  8. Au-Kline syndrome 
    ... Breckpot J, Devriendt K, Wierenga K, Fanning E, Grange DK, Graham GE, Galarreta C, Jones MC, Kini U, Stewart H, Parboosingh JS, Kline AD, Innes AM; Care for Rare Canada Consortium. Phenotypic spectrum of Au-Kline syndrome: a report of six new cases and review ...
    https://medlineplus.gov/genetics/condition/au-kline-syndrome - Genetics
  9. Wiedemann-Rautenstrauch syndrome 
    ... Xing C, Agarwal AK, Vergano SAS, Patel C, Grange DK, Kenney A, Najaf T, Nickerson DA, Bamshad MJ, Cole FS, Garg A. Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. Am J Hum Genet. 2018 Dec 6;103( ...
    https://medlineplus.gov/.../wiedemann-rautenstrauch-syndrome - Genetics
  10. HNRNPK gene 
    ... Breckpot J, Devriendt K, Wierenga K, Fanning E, Grange DK, Graham GE, Galarreta C, Jones MC, Kini U, Stewart H, Parboosingh JS, Kline AD, Innes AM; Care for Rare Canada Consortium. Phenotypic spectrum of Au-Kline syndrome: a report of six new cases and review ...
    https://medlineplus.gov/genetics/gene/hnrnpk - Genetics
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