Spectrum of Hereditary Ataxia in Omani Children
Amal Al-Habsi, Khalid Al-Thihli, Eiman Al-Ajmi, Amna Al-Futaisi, Abdullah Al-Badi, Fatema Al-Amrani · 2026
Read Spectrum of Hereditary Ataxia in Omani Children by Amal Al-Habsi, Khalid Al-Thihli, Eiman Al-Ajmi, Amna Al-Futaisi, Abdullah Al-Badi, Fatema Al-Amrani (2026) in the Tower of Babel, a free online library of public-domain works preserved in clean, searchable text. No sign-up. The full text is served as a plain-text file at a predictable URL, where text is present: https://antarctic-labs.com/tower-of-babel/pmc-13607818.txt.
Description
Amal Al-Habsi and five co-authors charted inherited ataxias in Omani children in 2026. These balance and coordination disorders spring from many genes and look alike at first, so diagnosis drags. The team reviewed ten years of cases at a university hospital in Oman for children under eighteen.
Records yielded patterns across symptoms, family history, brain scans, and gene tests. Some cases carried confirmed gene findings; others rested on clinical signs alone. The authors weigh which early clues best predict a confirmed diagnosis, aiming to shorten the diagnostic road for families in the region.
Catalog record
| CREATOR | Amal Al-Habsi, Khalid Al-Thihli, Eiman Al-Ajmi, Amna Al-Futaisi, Abdullah Al-Badi, Fatema Al-Amrani |
|---|---|
| YEAR | 2026 |
| COLLECTION | PAPERS |
| FORMAT | TXT |
| FILE SIZE | 33 KB |
| VERSION | 1.0 |
| LICENSE | CC BY 4.0 |
| RIGHTS | CC BY |
| SOURCE | Europe PMC |