A rare case of anophthalmia without any family history and antenatal risk factors

Anophthalmia is a rare genetic disorder. It is defined as the absence of one or both eyes in a patient. It can be unilateral or bilateral. Based on the absence of anatomical structures, it is divided into primary, secondary, and degenerative anophthalmia. It occurs in an infant with a diabetic mothe...

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Detalles Bibliográficos
Autores principales: Dedushi, Kreshnike, Hyseni, Fjolla, Musa, Juna, Saliaj, Kristi, Vokshi, Valon, Guy, Ali, Bhatti, Atiq, Rahman, Abdur, Tahir, Muhammad, Rakovica, Loran, Rahman, Masum, Shatri, Jeton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493492/
https://www.ncbi.nlm.nih.gov/pubmed/34630815
http://dx.doi.org/10.1016/j.radcr.2021.09.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493492/
https://www.ncbi.nlm.nih.gov/pubmed/34630815
http://dx.doi.org/10.1016/j.radcr.2021.09.001

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