Colonic Perforation in a Term Newborn with Hereditary Protein C Deficiency

被引：0

作者：

Hiroshi Mizumoto

Miki Kimura

Daisuke Hata

机构：

[1] Tazuke Kofukai Medical Research Institute,Department of Pediatrics, Kitano Hospital

来源：

Indian Pediatrics | 2019年 / 56卷

关键词：

D O I：

暂无

中图分类号：

学科分类号：

摘要：

We describe a term infant who experienced recurrent apnea associated with intracranial hemorrhage and later, developed colonic perforation. Plasma protein C activity was below detectable limits and a heterozygous PROC mutation was identified. Neonatal colonic perforation is rare, and this case report highlights the importance of considering congenital Protein C deficiency.

引用

页码：1057 / 1059

页数：2

共 50 条

[31] COUMARIN NECROSIS ASSOCIATED WITH HEREDITARY PROTEIN-C DEFICIENCY
MCGEHEE, WG
KLOTZ, TA
EPSTEIN, DJ
RAPAPORT, SI
ANNALS OF INTERNAL MEDICINE, 1984, 101 (01) : 59 - 60
[32] HOMOZYGOUS PROTEIN-C DEFICIENCY IN A NEWBORN - CLINICOPATHOLOGIC CORRELATION
TARRAS, S
GADIA, C
MEISTER, L
ROLDAN, E
GREGORIOS, JB
ARCHIVES OF NEUROLOGY, 1988, 45 (02) : 214 - 216
[33] SEVERE PROTEIN-C DEFICIENCY IN NEWBORN-INFANTS
MANCOJOHNSON, MJ
MARLAR, RA
JACOBSON, LJ
HAYS, T
WARADY, BA
JOURNAL OF PEDIATRICS, 1988, 113 (02): : 359 - 363
[34] Diagnostic challenge of the newborn patients with heritable protein C deficiency
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
Journal of Perinatology, 2019, 39 : 212 - 219
[35] Diagnostic challenge of the newborn patients with heritable protein C deficiency
Ichiyama, Masako
Inoue, Hirosuke
Ochiai, Masayuki
Ishimura, Masataka
Shiraishi, Akira
Fujiyoshi, Junko
Yamashita, Hironori
Sato, Kazuo
Matsumoto, Shinya
Hotta, Taeko
Uchiumi, Takeshi
Kang, Dongchon
Ohga, Shouichi
JOURNAL OF PERINATOLOGY, 2019, 39 (02) : 212 - 219
[36] HEREDITARY FUNCTIONAL PROTEIN C AND PROTEIN S DEFICIENCY IN A COHORT OF THROMBOPHILIC PATIENTS
Ionita, M.
Pacurar, R.
Ionita, H.
Nicola, D.
Cheveresan, L.
Ionita, I.
Cheveresan, M.
Tanasie, D.
Suceava, I.
Calamar, D.
Balgradean, S.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 : 516 - 516
[37] PURPURA FULMINANS IN A NEWBORN WITH HEREDITARY VITAMIN-C-DEFICIENCY - SUCCESSFUL TREATMENT WITH PHENPROCOUMON
WEHINGER, H
GEIGER, E
FREUDENBERG, V
SCHURMANN, J
ALEXANDRAKIS, E
WITT, I
MONATSSCHRIFT KINDERHEILKUNDE, 1984, 132 (09) : 749 - 749
[38] DETERMINATION OF PROTEIN-C IN THE EUTROPHIC NEWBORN AT TERM
POLACK, B
POUZOL, P
AMIRAL, J
KOLODIE, L
NOUVELLE REVUE FRANCAISE D HEMATOLOGIE, 1984, 26 (03): : 130 - 130
[39] A NEW KIND OF PROTEIN-C-DEFICIENCY IN NEONATES INTERMITTENT TREATMENT WITH PROTEIN-C-CONCENTRATE OF HEREDITARY TEMPORARY NEONATAL PROTEIN-C-DEFICIENCY
KREUZ, W
BEEG, T
THROMBOSIS AND HAEMOSTASIS, 1995, 73 (06) : 1293 - 1293
[40] Identification of mutations in 15 Hungarian families with hereditary protein C deficiency
Dávid, M
Losonczy, H
Sas, G
Nagy, A
Kutscher, G
Meyer, M
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 111 (01) : 129 - 135

← 1 2 3 4 5 →