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	»	Oculocutaneous Albinism (OCA)
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	»	Incontinentia Pigmenti (Bloch–Sulzberger Syndrome)
	»	Piebaldism
	»	Waardenburg Syndrome
»	Disorders with Pigmented Lesions
	»	McCune–Albright Syndrome (Polyostotic Fibrous Dysplasia)
	»	Russell–Silver Syndrome
»	Vascular Disorders
	»	Sturge–Weber Syndrome (SWS)
	»	Klippel–Trénaunay Syndrome (KTS)
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	»	Von Hippel–Lindau Syndrome (VHL)
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	»	Blue Rubber Bleb Nevus Syndrome (Bean Syndrome)
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	»	Hereditary Lymphedema (Milroy Disease)
	»	Lymphedema–Distichiasis Syndrome
	»	Noonan Syndrome
	»	Turner Syndrome
	»	Meige Lymphedema (Hereditary Lymphedema II)

McCune–Albright Syndrome (Polyostotic Fibrous Dysplasia)

Sporadic, GNAS 1 gene mutation, encodes α subunit of Gs adenylate cyclase
Large café-au-lait macules (geographic border), precocious puberty, pathological fractures, endocrine abnormalities (hyperparathyroidism, hyperthyroidism, acromegaly), sclerosis at base of skull


	MCCune – Café au lait macules, preCocious puberty; do NOT confuse with Albright hereditary osteodystrophy (pseudohypoparathyroidism)