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Chromosome 1q Terminal Deletion and Congenital Glaucoma: A Case Report
Patient: Female, 8-year-old Final Diagnosis: Chromosome 1 q31 and q42.1 deletion with congenital glaucoma Symptoms: Vision loss Medication: — Clinical Procedure: — Specialty: Ophthalmology OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: This paper aims to highlight the presence of p...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
International Scientific Literature, Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977633/ https://www.ncbi.nlm.nih.gov/pubmed/31927558 http://dx.doi.org/10.12659/AJCR.918128 |