Diagnostic challenge of the newborn patients with heritable protein C deficiency

被引：0
|
作者：
Masako Ichiyama
Hirosuke Inoue
Masayuki Ochiai
Masataka Ishimura
Akira Shiraishi
Junko Fujiyoshi
Hironori Yamashita
Kazuo Sato
Shinya Matsumoto
Taeko Hotta
Takeshi Uchiumi
Dongchon Kang
Shouichi Ohga
机构：
[1] Comprehensive Maternity and Perinatal Care Center,Department of Pediatrics, Graduate School of Medical Sciences
[2] Kyushu University Hospital,Department of Perinatal and Pediatric Medicine, Graduate School of Medical Sciences
[3] Kyushu University,Division of Pediatrics
[4] Kyushu University,Division of Pediatrics
[5] National Hospital Organization Kokura Medical Center,Department of Clinical Chemistry and Laboratory Medicine
[6] National Hospital Organization Kyushu Medical Center,undefined
[7] Kyushu University Hospital,undefined
来源：
Journal of Perinatology | 2019年 / 39卷
关键词：
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：212 / 219
页数：7
相关论文
共 50 条
  • [21] Diagnostic challenge of large congenital liver cyst in the newborn
    Viswanathan, Sreekanth
    Kumar, Deepak
    PEDIATRICS INTERNATIONAL, 2014, 56 (02) : 267 - 270
  • [22] SEVERE INHERITED HOMOZYGOUS PROTEIN-C DEFICIENCY IN A NEWBORN-INFANT
    ESTELLES, A
    GARCIAPLAZA, I
    DASI, A
    AZNAR, J
    DUART, M
    SANZ, G
    PEREZREQUEJO, JL
    ESPANA, F
    JIMENEZ, C
    ABELEDO, G
    THROMBOSIS AND HAEMOSTASIS, 1984, 52 (01) : 53 - 56
  • [23] HOMOZYGOUS PROTEIN-C DEFICIENCY MANIFESTED BY MASSIVE VENOUS THROMBOSIS IN THE NEWBORN
    SELIGSOHN, U
    BERGER, A
    ABEND, M
    RUBIN, L
    ATTIAS, D
    ZIVELIN, A
    RAPAPORT, SI
    NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (09): : 559 - 562
  • [24] PORTAL-VEIN THROMBOSIS IN NEWBORN DUE TO PROTEIN-C DEFICIENCY
    MORI, PG
    BORI, E
    MOLINARI, AC
    IASONNI, V
    DODERO, P
    CAFFARENA, PE
    AMATO, S
    ODINO, S
    PEDIATRIC RESEARCH, 1994, 36 (01) : A30 - A30
  • [25] Multiple congenital vascular lesions in a newborn: a diagnostic challenge
    Tejedor, Maria
    Gracia-Darder, Ines
    Balliu, Pere Ramon
    Asensio, Rafael Felix Ramos
    Jarque, Pilar
    Martin-Santiago, Ana
    ARCHIVES OF DISEASE IN CHILDHOOD, 2023, 108 (07) : 530 - 530
  • [26] Blueberry Muffin Syndrome and Hyperleukocytosis in a Newborn: A Diagnostic Challenge
    Teixeira, Beatriz
    Losa, Ana
    Meireles, Andreia
    Lachado, Ana
    Guerra, Isabel Couto
    Machado, Susana
    Branco, Lidia
    Paulino, Paulo
    Lau, Catarina
    Oliva-Teles, Natalia
    Mendes, Carlos
    Oliva, Tereza
    Pinho, Liliana
    Neiva, Luisa
    Proenca, Elisa
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (01)
  • [27] Protein C deficiency in critically ill patients
    Yaguchi, A
    Clausi, C
    Bruhn, A
    Akieda, K
    Vincent, JL
    Pradier, O
    CRITICAL CARE MEDICINE, 2005, 33 (12) : A151 - A151
  • [28] Attitudes toward genetic testing for thrombophilia in asymptomatic members of a large family with heritable protein C deficiency
    Van Korlaar, IM
    Vossen, CY
    Rosendaal, FR
    Bovill, EG
    Naud, S
    Cameron, LD
    Kaptein, AA
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2005, 3 (11) : 2437 - 2444
  • [29] POPULATION PHARMACOKINETICS OF INTRAVENOUS PROTEIN C CONCENTRATE IN PATIENTS WITH PROTEIN C DEFICIENCY
    Chu, L-H
    Sorribes, I. C.
    Taylor, A.
    Schneider, J.
    Li, Z.
    HAEMOPHILIA, 2023, 29 : 172 - 173
  • [30] Staphylococcal endocarditis as the first manifestation of heritable protein S deficiency in childhood
    Hoshina, Takayuki
    Nakashima, Yasutaka
    Sato, Daisuke
    Nanishi, Etsuro
    Nishio, Hisanori
    Nagata, Hazumu
    Yamamura, Kenichiro
    Doi, Takehiko
    Shiokawa, Yuichi
    Koga, Yui
    Kang, Dongchon
    Ohga, Shouichi
    Hara, Toshiro
    JOURNAL OF INFECTION AND CHEMOTHERAPY, 2014, 20 (1-2) : 128 - 130
12345