Melanocytic Disorders

Oculocutaneous albinism: lack of melanin in skin, hair and eyes, high skin cancer risk, and how Haute-Derma screens and protects the skin long term.

Genetic pigmentation disorders such as piebaldism, Waardenburg syndrome, incontinentia pigmenti and NF1 café-au-lait spots: diagnosis and care at Haute-Derma.

• Hermansky-Pudlak Syndrome
• Chédiak-Higashi Syndrome
• Incontinentia Pigmenti
• Piebaldism
• Waardenburg Syndrome
• Tietz Syndrome
• Symmetrical Dyschromatosis
• Diffuse Mixed Pigmentation Disorder
• Kitamura Pigmentary Disorder
• Dowling–Degos Disease

Vitiligo explained: why white patches form, active vs. stable disease, JAK inhibitor creams, excimer light and cell grafting options at Haute-Derma.

Hypermelanosis explained: why skin darkens, how epidermal and dermal pigment differ, related conditions, and multi-target treatment at Haute-Derma.

• Linear & Whorled Nevoid Hypermelanosis – LWNH
• Naegeli-Franceschetti-Jadassohn Syndrome
• Haber Syndrome
• Nevus of Ota
• Nevus of Ito
• Mongolian Spots
• Familial Café-Au-Lait Syndromes
• Nelson Syndrome
• Pheochromocytoma
• Carcinoid Syndrome
• Hyperthyroidism
• Maturational Dyschromia
• Ochronosis
• Pigmentary Demarcation Lines
• Acquired Idiopathic Facial Pigmentation
• Periorbital Pigmentation
• Mucosal Hyperpigmentation
• Acral Hyperpigmented Macules
• Freckles (Ephelides)
• Prurigo Pigmentosa
• Nevus of Hori
• Becker Nevus
• Café-au-lait Macules
• Acromelanosis Progressiva
• Post-Inflammatory Hyperpigmentation
• Melasma
• Partial Unilateral Lentiginosis
• Erythema Ab Igne
• Riehl Melanosis
• Cronkhite-Canada Syndrome
• Erythrose Péribuccale Pigmentaire of Brocq
• Erythema dyschromicum perstans
• Lichen Planus Pigmentosus