A Rare Case Report of 17q23.1q23.2 Microdeletion With Homozygosity of 11p11.2q13.4 in a Newborn

We present the case of a newborn with 17q23.1q23.2 microdeletion and additional homozygosity of 11p11.2q13.4. In the literature, 17q23.1q23.2 microdeletion syndrome is a novel syndrome reported in nine patients. Our patient is a full-term baby boy admitted to a neonatal intensive care unit for hypog...

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Detalles Bibliográficos
Autores principales: Barola, Sindhu, Parrill, Allison M, Mahmoudzadeh, Samaan, Bizargity, Peyman, Verma, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012598/
https://www.ncbi.nlm.nih.gov/pubmed/35449653
http://dx.doi.org/10.7759/cureus.23290

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012598/
https://www.ncbi.nlm.nih.gov/pubmed/35449653
http://dx.doi.org/10.7759/cureus.23290

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