Clinical Presentation of Congenital Heterochromia Iridis in Pakistani Patients
Heterochromia iridis is a rare genetic disorder, characterized by variation in the concentration and distribution of the melanin pigment. It is caused by mutation in genes responsible for the synthesis of melanin pigment iris of the eye. Heterochromia Iridis is inherited as a simple Mendelian trait...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
ziauddin University
2024-10-01
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| Serie: | Pakistan Journal of Medicine and Dentistry |
| Soggetti: | |
| Accesso online: | https://ojs.zu.edu.pk/pjmd/article/view/3114 |
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