| • | autosomal dominant; Moynihan’s syndrome; multiple lentigines syndrome; mucous membranes generally spared |
| • | E – EKG abnormalities (conduction defects) |
| • | O – ocular hypertelorism |
| • | A – abnormal genitalia (hyperspadia, cryptorchidism) |
| • | R – retardation of growth |
| • | D –sensorineural deafness |
|
| • | M – mucocutaneous myxoma |
|
| • | M – mucocutaneous myxomas |
|
| • | I – intellectual impairment |
| • | B – brittle hair (= trichothiodystrophy; hair, low cysteine content (sulfur amino acid) tigertail when polarized) |
|
| • | K – keratitis (ocular: can cause blindness) |
|
| • | S – skin changes (hyperpigmentation, hypertrichotic, sclerodermatous, glomeruloid hemangioma) |
| • | AKA osteosclerotic myeloma (in plasma cell dyscrasia category) |
|
| • | CH – congenital hemidysplasia |
| • | I – ichthyosis erythroderma (following Blashckos lines) |
| • | X-linked dominant (therefore follows Blashko’s lines) |
|
| • | AN – acanthosis nigricans |
|
|
