Clinical and genetic characteristics of De Novo Tetrasomy 18p in early infancy: A case report
Introduction: Tetrasomy 18p is a rare chromosomal disorder caused by the presence of an isochromosome consisting of two copies of the short arm of chromosome 18, resulting in four copies of 18p It is typically sporadic and presents with a wide spectrum of clinical manifestations, including developme...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2026-06-01
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| Serie: | Global Pediatrics |
| Soggetti: | |
| Accesso online: | http://www.sciencedirect.com/science/article/pii/S266700972600014X |
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