Epidermal nevus syndrome

Epidermal nevus syndrome, also known as Feuerstein and Mims syndrome,^[1][2] and Solomon's syndrome^{[1]: 775 [3]} is a rare disease that was first described in 1968 and consists of extensive epidermal nevi with abnormalities of the central nervous system (CNS), skeleton, skin, cardiovascular system, genitourinary system and eyes.^[2]: 634 However, since the syndrome's first description, a broader concept for the "epidermal nevus" syndrome has been proposed, with at least six types being described:^{[1]: 776 [4]}

• Schimmelpenning syndrome
• Nevus comedonicus syndrome
• Pigmented hairy epidermal nevus syndrome
• Proteus syndrome
• CHILD syndrome
• Phakomatosis pigmentokeratotica

Other namesSolomon's syndrome, Feuerstein and Mims syndrome

SpecialtyDermatology, medical genetics 

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Epidermal nevus syndrome
Other names	Solomon's syndrome, Feuerstein and Mims syndrome
Epidermal nevus in lower eyelid margin
Specialty	Dermatology, medical genetics

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