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Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding.
Kharel, Sanjeev; Koirala, Dinesh Prasad; Shrestha, Suraj; Sedai, Hari; Shrestha, Bibek Man; Homagain, Sushan; Kandel, Suraj.
  • Kharel S; Institute of Medicine Maharajgunj Medical Campus Kathmandu Nepal.
  • Koirala DP; Department of Gastrointestinal and General Surgery Pediatric Surgery Unit Tribhuvan University Teaching Hospital Kathmandu Nepal.
  • Shrestha S; Institute of Medicine Maharajgunj Medical Campus Kathmandu Nepal.
  • Sedai H; Institute of Medicine Maharajgunj Medical Campus Kathmandu Nepal.
  • Shrestha BM; Institute of Medicine Maharajgunj Medical Campus Kathmandu Nepal.
  • Homagain S; Institute of Medicine Maharajgunj Medical Campus Kathmandu Nepal.
  • Kandel S; Institute of Medicine Maharajgunj Medical Campus Kathmandu Nepal.
Clin Case Rep ; 9(8): e04573, 2021 Aug.
Article en En | MEDLINE | ID: mdl-34401157
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Article