REFERENCES

1. Messina C. Woodhouse-Sakati syndrome: a review. Rev Neurol. 2025;181:21-30.

2. Ali R, Al-Dewik N, Mohammed S, et al. Expanding on the phenotypic spectrum ofWoodhouse-Sakatisyndrome due to founder pathogenic variant in DCAF17: report of 58 additional patients from Qatar and literature review. Am J Med Genet A. 2022;188:116-29.

3. Kohil A, Abdallah AM, Hussain K, Al-Shafai M. Genetic epidemiology of Woodhouse-Sakati Syndrome in the Greater Middle East region and beyond: a systematic review. Orphanet J Rare Dis. 2023;18:22.

4. Agopiantz M, Corbonnois P, Sorlin A, et al. Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature. J Endocrinol Invest. 2014;37:1-7.

5. Jagota P, Ugawa Y, Aldaajani Z, et al. Nine hereditary movement disorders first described in asia: their history and evolution. J Mov Disord. 2023;16:231-47.

6. Bakhsh H, Alqntash N, Almajed E. The successful management of primary amenorrhea in Woodhouse-Sakati syndrome: a case report and a literature review. Life. 2023;13:2022.

7. Zhou M, Shi N, Zheng J, et al. Case report: a Chinese family of Woodhouse-Sakati syndrome with diabetes mellitus, with a novel biallelic deletion mutation of the DCAF17 gene. Front Endocrinol. 2021;12:770871.

8. Fleseriu M, Hashim IA, Karavitaki N, et al. Hormonal replacement in hypopituitarism in adults: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2016;101:3888-921.

9. Aljaffer MA, Almadani AH, Almutlaq M, Alhammad A, Alyahya AS. Woodhouse-Sakati syndrome presenting with psychotic features after starting trihexyphenidyl: a case report. Cureus. 2022;14;e27576.

10. Amosova M, Poluboyarinova I, Fadeev V, Asanov A. Woodhouse-Sakati syndrome: the new genetic variant of DCAF17 in 2 adult sisters. JCEM Case Rep. 2024;2:luae130.

11. Bohlega S, Abusrair AH, Al-Ajlan FS, et al. Patterns of neurological manifestations in Woodhouse-Sakati syndrome. Parkinsonism Relat Disord. 2019;69:99-103.

12. Schneider SA, Bhatia KP. Dystonia in the Woodhouse Sakati syndrome: a new family and literature review. Mov Disord. 2008;23:592-6.

13. Khalili Dehkordi A, Vakili R. DCAF17 mutation in Woodhouse-Sakati syndrome: a case report on a novel homozygous variant. Case Rep Pediatr. 2025;2025:9913412.

14. Alhuzaim ON, Ahmad MM, Sherbeeni SM, Almotawa F, Ali AS, Alhejaily AG. Three siblings with Woodhouse-Sakati syndrome: a case report of a new Saudi family. Cureus. 2022;14:e32225.

15. Khosravi S, Moosavian T, Salehpour S, Habibi SAH, Alavi A, Rohani M. Clinical and genetic characterization of Woodhouse-Sakati syndrome in Iranian patients: a case series. J Mov Disord. 2025;18:257-61.

16. Noble M, Cahill D. Hypogonadism: cardiometabolism and gonadal function in men. Metab Target Organ Damage. 2024;4:14.

17. Amalnath SD, Jothivanan, Oshima J, Buchan JG, Paolucci S. Woodhouse-Sakati syndrome in an Indian patient with a novel pathogenic variant. Am J Med Genet A. 2024;194:100-2.