Page last updated: 2024-10-31

apnea and Hirschsprung Disease

apnea has been researched along with Hirschsprung Disease in 5 studies

Apnea: A transient absence of spontaneous respiration.

Hirschsprung Disease: Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON.

Research Excerpts

ExcerptRelevanceReference
" The patient's clinical manifestations were apnea and cyanosis requiring immediate endotracheal intubation, recurrent hypoventilation with hypercapnia, hypoxia after ventilator removal, and abdominal distension since birth."3.77PHOX2B mutations in patients with Ondine-Hirschsprung disease and a review of the literature. ( Chang, YS; Ki, CS; Kim, JW; Kim, JY; Kwon, MJ; Lee, GH; Lee, MK; Park, WS; Yoo, HS, 2011)
"The main symptoms were abdominal distension (n = 10), vomiting (n = 6), constipation (n = 2), and apnea (n = 1)."3.77Importance of evaluating for cow's milk allergy in pediatric surgical patients with functional bowel symptoms. ( Etani, Y; Ida, S; Ikeda, K; Kawahara, H; Kawamoto, K; Kubota, A, 2011)
"This report presents an otherwise healthy infant who developed unexplained apnea and long-segment Hirschsprung disease."3.74Haddad syndrome: a case of an infant with central congenital hypoventilation syndrome and Hirschsprung disease. ( Lai, D; Schroer, B, 2008)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kwon, MJ1
Lee, GH1
Lee, MK1
Kim, JY1
Yoo, HS1
Ki, CS1
Chang, YS1
Kim, JW1
Park, WS1
Listernick, R1
Ikeda, K1
Ida, S1
Kawahara, H1
Kawamoto, K1
Etani, Y1
Kubota, A1
Yanes-Vidal, GJ1
García-Perla, JL1
Alarcón-Rubio, M1
Martinez-Canguelossi, S1
Lai, D1
Schroer, B1

Other Studies

5 other studies available for apnea and Hirschsprung Disease

ArticleYear
PHOX2B mutations in patients with Ondine-Hirschsprung disease and a review of the literature.
    European journal of pediatrics, 2011, Volume: 170, Issue:10

    Topics: Apnea; Biomarkers; Cyanosis; Exons; Genotype; Hirschsprung Disease; Homeodomain Proteins; Humans; Hy

2011
Male infant with shallow respirations.
    Pediatric annals, 2011, Volume: 40, Issue:10

    Topics: Apnea; Cyanosis; Hirschsprung Disease; Homeodomain Proteins; Humans; Hypoventilation; Infant; Infant

2011
Importance of evaluating for cow's milk allergy in pediatric surgical patients with functional bowel symptoms.
    Journal of pediatric surgery, 2011, Volume: 46, Issue:12

    Topics: Animals; Apnea; Catheterization; Cattle; Constipation; Diagnosis, Differential; Diagnostic Errors; E

2011
Apnoea episodes in Hirschsprung's disease and the anaesthesia implications of neurocristopathies.
    Paediatric anaesthesia, 2004, Volume: 14, Issue:3

    Topics: Anesthesia; Apnea; Child, Preschool; Hirschsprung Disease; Humans; Male; Postoperative Complications

2004
Haddad syndrome: a case of an infant with central congenital hypoventilation syndrome and Hirschsprung disease.
    Journal of child neurology, 2008, Volume: 23, Issue:3

    Topics: Abnormalities, Multiple; Apnea; DNA Repeat Expansion; Hirschsprung Disease; Homeodomain Proteins; Hu

2008