Molecular Vision: Sharon, Mol Vis 2015; 21:783-792. Table 1

Table 1. Mode of inheritance patterns in the studied set of patients.

Analyzed cohort	No. of recruited families (No. of patients)**	AR	Isolate cases, from consanguineous families	AD	XL	Isolate cases
Based on family history*	183 (383)	70 (38%)	32 (17%)	15 (8%)	12 (7%)	54 (30%)
Updated following genetic evaluation*	183 (383)	90 (49%)	26 (14%)	15 (8%)	12 (7%)	40 (22%)
Arab Muslims	66 (151)	36 (55%)	17 (26%)	2 (3%)	3 (4%)	8 (12%)
Jews	116 (227)	54 (46%)	10 (9%)	13 (11%)	8 (7%)	31 (27%)

*The inheritance pattern in each family was initially determined by the family history (first row- “Based on family history”). Following the genetic diagnosis (in 35% of cases), the inheritance pattern was revised based on the identified gene and mutation (second row- “Updated following genetic evaluation“), resulting in more accurate values. **- The total number of patients (383) includes mainly patients of Arab-Muslim origin (151) and Jewish origin (227), as well as 5 patients (who belong to the same family) of Bedouin origin.