Review of literature: case reports of coexistence of congenital adrenal hyperplasia and type-1-diabetes mellitus
| Case report . | CAH diagnosis (year) . | T1DM diagnosis (year) . | Comorbidity . |
|---|---|---|---|
| Islam et al. (3) | at birth | 11 yo at routine exams (plasma glucose of 596 mg/dL) | Brother with CAH, no family history for autoimmune diseases |
| Islam et al. (3) | 2 weeks after birth. | 2 weeks after birth at routine exams (blood glucose level 710 mg/dL) | No familial history both for CAH and T1DM |
| Positive neonatal screening | |||
| Aureli et al. (10) | 6.5 y/o (non classical CAH) | 16 y/o, diabetic ketoacidosis (plasma glucose of 382 mg/dL) | Prader–Willi syndrome, central precocious puberty, no family history for autoimmune diseases |
| Zachariah et al. (11) | 4 y/o (non classical CAH) | 15 y/o, diabetic ketoacidosis (plasma glucose of 55 mg/dL) | - |
| Case report . | CAH diagnosis (year) . | T1DM diagnosis (year) . | Comorbidity . |
|---|---|---|---|
| Islam et al. (3) | at birth | 11 yo at routine exams (plasma glucose of 596 mg/dL) | Brother with CAH, no family history for autoimmune diseases |
| Islam et al. (3) | 2 weeks after birth. | 2 weeks after birth at routine exams (blood glucose level 710 mg/dL) | No familial history both for CAH and T1DM |
| Positive neonatal screening | |||
| Aureli et al. (10) | 6.5 y/o (non classical CAH) | 16 y/o, diabetic ketoacidosis (plasma glucose of 382 mg/dL) | Prader–Willi syndrome, central precocious puberty, no family history for autoimmune diseases |
| Zachariah et al. (11) | 4 y/o (non classical CAH) | 15 y/o, diabetic ketoacidosis (plasma glucose of 55 mg/dL) | - |
Review of literature: case reports of coexistence of congenital adrenal hyperplasia and type-1-diabetes mellitus
| Case report . | CAH diagnosis (year) . | T1DM diagnosis (year) . | Comorbidity . |
|---|---|---|---|
| Islam et al. (3) | at birth | 11 yo at routine exams (plasma glucose of 596 mg/dL) | Brother with CAH, no family history for autoimmune diseases |
| Islam et al. (3) | 2 weeks after birth. | 2 weeks after birth at routine exams (blood glucose level 710 mg/dL) | No familial history both for CAH and T1DM |
| Positive neonatal screening | |||
| Aureli et al. (10) | 6.5 y/o (non classical CAH) | 16 y/o, diabetic ketoacidosis (plasma glucose of 382 mg/dL) | Prader–Willi syndrome, central precocious puberty, no family history for autoimmune diseases |
| Zachariah et al. (11) | 4 y/o (non classical CAH) | 15 y/o, diabetic ketoacidosis (plasma glucose of 55 mg/dL) | - |
| Case report . | CAH diagnosis (year) . | T1DM diagnosis (year) . | Comorbidity . |
|---|---|---|---|
| Islam et al. (3) | at birth | 11 yo at routine exams (plasma glucose of 596 mg/dL) | Brother with CAH, no family history for autoimmune diseases |
| Islam et al. (3) | 2 weeks after birth. | 2 weeks after birth at routine exams (blood glucose level 710 mg/dL) | No familial history both for CAH and T1DM |
| Positive neonatal screening | |||
| Aureli et al. (10) | 6.5 y/o (non classical CAH) | 16 y/o, diabetic ketoacidosis (plasma glucose of 382 mg/dL) | Prader–Willi syndrome, central precocious puberty, no family history for autoimmune diseases |
| Zachariah et al. (11) | 4 y/o (non classical CAH) | 15 y/o, diabetic ketoacidosis (plasma glucose of 55 mg/dL) | - |
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