Hypocalcemia and Graves' disease associated with 22q11.2 deletion syndrome

被引：0
|
作者：
Tanaka, Wataru [1 ]
Oyama, Noriko [1 ,2 ]
Makimura, Mika [1 ]
Miyako, Kenichi [1 ]
机构：
[1] Fukuoka Childrens Hosp, Dept Endocrinol & Metab, Fukuoka, Japan
[2] Oita Prefectural Hosp, Dept Pediat, 2-8-1 Bunyou, Oita 8700855, Japan
来源：
PEDIATRICS INTERNATIONAL | 2023年 / 65卷 / 01期
关键词：
22q11.2 deletion syndrome; Graves' disease; hypocalcemia;
D O I：
10.1111/ped.15709
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
[No abstract available]
引用
收藏
页数：2
相关论文
共 50 条
  • [41] 22q11.2 deletion syndrome in diverse populations
    Kruszka, Paul
    Addissie, Yonit A.
    McGinn, Daniel E.
    Porras, Antonio R.
    Biggs, Elijah
    Share, Matthew
    Crowley, T. Blaine
    Chung, Brian H. Y.
    Mok, Gary T. K.
    Mak, Christopher C. Y.
    Muthukumarasamy, Premala
    Thong, Meow-Keong
    Sirisena, Nirmala D.
    Dissanayake, Vajira H. W.
    Paththinige, C. Sampath
    Prabodha, L. B. Lahiru
    Mishra, Rupesh
    Shotelersuk, Vorasuk
    Ekure, Ekanem Nsikak
    Sokunbi, Ogochukwu Jidechukwu
    Kalu, Nnenna
    Ferreira, Carlos R.
    Duncan, Jordann-Mishael
    Patil, Siddaramappa Jagdish
    Jones, Kelly L.
    Kaplan, Julie D.
    Abdul-Rahman, Omar A.
    Uwineza, Annette
    Mutesa, Leon
    Moresco, Angelica
    Gabriela Obregon, Maria
    Richieri-Costa, Antonio
    Gil-da-Silva-Lopes, Vera L.
    Adeyemo, Adebowale A.
    Summar, Marshall
    Zackai, Elaine H.
    McDonald-McGinn, Donna M.
    Linguraru, Marius George
    Muenke, Maximilian
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (04) : 879 - 888
  • [42] Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome
    McLean-Tooke, A.
    Spickett, G. P.
    Gennery, A. R.
    SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2007, 66 (01) : 1 - 7
  • [43] Autism in children with 22Q11.2 deletion syndrome
    Eliez, Stephan
    JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2007, 46 (04): : 433 - 434
  • [44] Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome
    Lima, Kari
    Abrahamsen, Tore G.
    Wolff, Anette Boe
    Husebye, Eystein
    Alimohammadi, Mohammad
    Kampe, Olle
    Folling, Ivar
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2011, 165 (02) : 345 - 352
  • [45] Opitz GBBB syndrome and the 22q11.2 deletion
    Lacassie, Y
    Arriaza, MI
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1996, 62 (03): : 318 - 318
  • [46] NEUROCOGNITIVE FUNCTIONING IN 22Q11.2 DELETION SYNDROME
    Gur, Raquel E.
    Emanuel, Beverly S.
    Yi, James J.
    McDonald-McGinn, Donna M.
    Tang, Sunny X.
    Zackai, Elaine H. J.
    Whinna, Daneen
    Souders, Margaret C.
    Calkins, Monica E.
    Kohler, Christian G.
    Savitt, Adam
    Gur, Ruben C.
    SCHIZOPHRENIA RESEARCH, 2014, 153 : S76 - S76
  • [47] HYPERPROLINEMIA AND PSYCHIATRY IN 22Q11.2 DELETION SYNDROME
    van Asbeck, E.
    Morava-Kozicz, E.
    JOURNAL OF INVESTIGATIVE MEDICINE, 2014, 62 (02) : 454 - 454
  • [48] Immunological aspects of 22q11.2 deletion syndrome
    A. R. Gennery
    Cellular and Molecular Life Sciences, 2012, 69 : 17 - 27
  • [49] Complement Activation in 22q11.2 Deletion Syndrome
    Dina Grinde
    Torstein Øverland
    Kari Lima
    Camilla Schjalm
    Tom Eirik Mollnes
    Tore G. Abrahamsen
    Journal of Clinical Immunology, 2020, 40 : 515 - 523
  • [50] Neuroradiographic findings in 22q11.2 deletion syndrome
    Bohm, Lauren A.
    Zhou, Tom C.
    Mingo, Tyler J.
    Dugan, Sarah L.
    Patterson, Richard J.
    Sidman, James D.
    Roby, Brianne B.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (08) : 2158 - 2165
12345