A Case Report of a Premature Infant With Coxsackie B1 Meningitis

2007 ◽  
Vol 7 (5) ◽  
pp. 238-247 ◽  
Author(s):  
Jennifer Callen ◽  
Bosco A. Paes
Keyword(s):  
2002 ◽  
Vol 22 (3) ◽  
pp. 252-254 ◽  
Author(s):  
Akira Harigaya ◽  
Yasushi Nako ◽  
Akihiro Morikawa ◽  
Hiroya Okano ◽  
Takeshi Takagi

Author(s):  
Ravi Teja Juloori ◽  
Febe Renjitha Suman ◽  
Rithika Rajendran ◽  
B Uma Maheswari

1998 ◽  
Vol 15 (01) ◽  
pp. 35-38 ◽  
Author(s):  
Nehama Linder ◽  
Nathan Keller ◽  
Chaim Huri ◽  
Jacob Kuint ◽  
Anna Goldshmidt-Reuven ◽  
...  

2009 ◽  
Vol 67 (1) ◽  
pp. 218-222 ◽  
Author(s):  
Belmiro Cavalcanti do Egito Vasconcelos ◽  
Carlos Augusto Pereira Lago ◽  
Ricardo Viana Bessa Nogueira ◽  
David Gomes de Alencar Gondim ◽  
Arnaldo Brito Filho

PEDIATRICS ◽  
1975 ◽  
Vol 56 (3) ◽  
pp. 459-462
Author(s):  
Robert J. Touloukian ◽  
Raymond Duncan

Hirschsprung's disease is presumably caused by intrauterine environmental or genetic factors which prevent the migration and formation of the intramural ganglion cell (IMG) in the distal colon. While the IMG is known to be particularly sensitive to anoxemia and other postnatal environmental factors, its selective loss following such stress has not been substantiated in an unoperated patient. The following report of a stressed premature newborn with the clinical and radiographic features of Hirschsprung's disease clearly documents the histologic disappearance of the IMG from the distal colon. CASE REPORT D.J. (#88-65-29), a 1,525-gm male infant, was born to a healthy 22-year-old abortus 0, gravida 1, para 0 mother following an uncomplicated 30-week gestation, ending in a spontaneous uncomplicated delivery.


JIMD Reports ◽  
2020 ◽  
Author(s):  
Oliver Heath ◽  
James Pitt ◽  
Simone Mandelstam ◽  
Carl Kuschel ◽  
Anand Vasudevan ◽  
...  

2012 ◽  
Vol 62 (1) ◽  
pp. 74-79
Author(s):  
Deb Sanjay Nag ◽  
Devi Prasad Samaddar ◽  
Pratap Rudra Mahanty ◽  
Aoyon Sengupta

2019 ◽  
Vol 65 (6) ◽  
pp. 638-641
Author(s):  
Mohammed A Alsuhaibani

Abstract Haemophilus parainfluenzae is an unusual causative organism of invasive bacterial infection in adults and children. Mortality and morbidity secondary to Haemophilus parainfluenzae have been documented in the literature. We present a rare case of a premature infant with early onset sepsis caused by Haemophilus parainfluenzae, who was born to a primigravida with chorioamnionitis. The infant was successfully treated for 10 days with antibiotics with no complications.


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