Table 1. Syndromes
associated with acanthosis nigricans[1, 4]
|
Insulin Resistance Syndromes |
|
Acral hypertrophy and muscle cramps[11] |
|
Acromegaly[12,
13] |
|
Alstrm syndrome[14] |
|
Ataxia-telangiectasia (Louis-Bar
syndrome)[15] |
|
Cushing syndrome[16] |
|
Diabetes Mellitus Type 2[2,
7, 17] |
|
Gonadal
dysfunction[7] |
|
Ovarian hyperthecosis[18] |
|
Polycystic ovary syndrome (PCOS,
Stein-Leventhal syndrome)[7] |
|
Hyperplasia of the adrenal
cortex, diabetes mellitus, and hypertrophy of the pineal body (Rabson-Mendenhall syndrome)[19] |
|
Leprechaunism[20] |
|
Lipodystrophy[21,
22] |
|
Congenital
lipodystrophic diabetes with acanthosis
nigricans (Lawrence-Seip
syndrome) |
|
Congenital
generalized lipodystrophy (Seip-Berardinelli
syndrome) |
|
Familial
partial lipodystrophy
(Kobberling-Dunnigan syndrome) |
|
Mental retardation,
overgrowth, remarkable faces, and acanthosis nigricans (MORFAN)[23] |
|
Prader-Willi syndrome[24] |
|
Type A syndrome (Hyperandrogenism, insulin resistance, and AN syndrome, or
HAIR-AN)[9] |
|
Type B syndrome[8] |
|
HashimotoÕs
thyroiditis |
|
Scleroderma |
|
SjgrenÕs
syndrome |
|
Systemic
lupus erythematosus[25] |
|
Type C syndrome |
|
Fibroblast Growth Factor Receptor Defect
Syndromes |
|
Beare-Stevenson cutis gyrata syndrome[26] |
|
CrouzonÕs syndrome with acanthosis nigricans[27] |
|
Severe achondroplasia
with developmental delay and acanthosis nigricans (SADDAN)[28] |
|
Thanatophoric dysplasia[29, 30] |
|
Other Associations |
|
Benign encephalopathy[31] |
|
Congenital adrenal hyperplasia[32] |
|
Costello syndrome[33,
34] |
|
Hepatolenticular degeneration (WilsonÕs disease)[35] |
|
Hirschowitz syndrome[1] |
|
Hypothyroidism[36] |
|
Kabuki syndrome[37] |
|
Ichthyosis with hypogonadism (RudÕs syndrome)[38] |
|
Primary biliary
cirrhosis[39] |