Kenny Caffey syndrome 2; expanding the clinical spectrum

被引:0
|
作者
Hatziagapiou, Kyriaki [1 ,2 ]
Sertedaki, Amalia [1 ,2 ]
Dermentzoglou, Vasiliki [3 ]
Kanaka-Gantenbein, Christina [1 ,2 ]
Sakka, Sophia D. [1 ,2 ]
机构
[1] Natl & Kapodistrian Univ Athens, Med Sch, ENDO ERN Ctr Rare Pediat Endocrine Disorders, Dept Pediat 1, Athens, Greece
[2] Natl & Kapodistrian Univ Athens, Med Sch, ENDO ERN Ctr Rare Pediat Endocrine Disorders, Dept Pediat 1,Aghia Sophia Childrens Hosp, Athens, Greece
[3] Aghia Sofia Childrens Hosp, Dept Radiol, Athens, Greece
来源
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P2-58
引用
收藏
页码:480 / 480
页数:1
相关论文
共 50 条
  • [1] Kenny Caffey syndrome with severe respiratory and gastrointestinal involvement: expanding the clinical phenotype
    Christodoulou, Loucas
    Krishnaiah, Anil
    Spyridou, Christina
    Salpietro, Vincenzo
    Hannan, Siobhan
    Saggar, Anand
    Mankad, Kshitij
    Deep, Akash
    Kinali, Maria
    QUANTITATIVE IMAGING IN MEDICINE AND SURGERY, 2015, 5 (03) : 476 - 479
  • [2] Expanding the Phenotypic Spectrum of Kenny-Caffey Syndrome (Withdrawn Publication. See MAR, 2023)
    Schigt, Heidi
    Bald, Martin
    van der Eerden, Bram C. J.
    Gal, Lars
    Ilenwabor, Barnabas P.
    Konrad, Martin
    Levine, Michael A.
    Li, Dong
    Mache, Christoph J.
    Mackin, Sharon
    Perry, Colin
    Rios, Francisco J.
    Schlingmann, Karl Peter
    Storey, Ben
    Trapp, Christine M.
    Verkerk, Annemieke J. M. H.
    Zillikens, M. Carola
    Touyz, Rhian M.
    Hoorn, Ewout J.
    Hoenderop, Joost G. J.
    de Baaij, Jeroen H. F.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2023, 108 (09): : E754 - E768
  • [3] Kenny-Caffey syndrome type 2
    Yerawar, C.
    Kabde, A.
    Deokar, P.
    QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2021, 114 (04) : 267 - 269
  • [4] Kenny-Caffey syndrome and microorchidism
    Hoffman, WH
    Kovacs, K
    Li, SB
    Kulharya, AS
    Johnson, BL
    Eidson, MS
    Cleveland, WW
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1998, 80 (02): : 107 - 111
  • [5] Kenny-Caffey Syndrome in the Neonatal Period
    Alves, M. Eduarda Caseiro
    Cadete, Vitoria
    Marques, Filipa
    Carneiro, Rita
    Neves, Joao Farela
    Galhardo, Julia
    HORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 342 - 342
  • [6] Kenny-Caffey syndrome: an Arab variant?
    Sabry, MA
    Farag, TI
    Shaltout, AA
    Zaki, M
    Al-Mazidi, Z
    Abulhassan, SJ
    Al-Torki, N
    Quishawi, A
    Al Awadi, SA
    CLINICAL GENETICS, 1999, 55 (01) : 44 - 49
  • [7] Expanding the phenotypic spectrum of Caffey disease
    Suphapeetiporn, K.
    Tongkobpetch, S.
    Mahayosnond, A.
    Shotelersuk, V.
    CLINICAL GENETICS, 2007, 71 (03) : 280 - 284
  • [8] Genotypic/phenotypic heterogeneity of Kenny-Caffey syndrome
    Sabry, MA
    Zaki, M
    Shaltout, A
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (12) : 1054 - 1055
  • [9] Kenny Caffey Syndrome; a Rare Diagnosis in Saudi Arabia
    Alzahrani, Hajer
    Babikr, Amir
    Alghamdi, Omair
    Almutairi, Fuad
    Al Alwan, Ibrahim
    HORMONE RESEARCH IN PAEDIATRICS, 2023, 96 : 488 - 488
  • [10] Oral manifestations of patients with Kenny-Caffey Syndrome
    Moussaid, Youssra
    Griffiths, Didier
    Richard, Beatrice
    Dieux, Anne
    Lemerrer, Martine
    Leger, Juliane
    Lacombe, Didier
    Bailleul-Forestier, Isabelle
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2012, 55 (8-9) : 441 - 445