Table 6.2-2. Differential diagnosis and treatment of MODY and type 1 diabetes mellitus

Differential features

MODY

Type 1 diabetes mellitus

Congenital malformations (most frequently affecting the kidneys and urogenital system)

Possible

No

≥3 generations of family history of diabetes mellitus at age <30 years

Yes

No

History/family history of autoimmune diseases

No

Yes

Islet cell antibodies

No

Yes

C-peptide level

Initially normal

Low

Treatment of choice

Initial treatment with sulfonylureas

Insulin

Onset

Slow and often asymptomatic

Usually acute

MODY, maturity-onset diabetes of youth.