
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Hypomelanosis
Introduction
Overview
Overview
Hypomelanosis is also referred to as hypopigmentation, and a condition in which there is too little pigment in the skin, hair, mucous membranes, and retina of the eye.
Causes
Causes
Common Causes
- Actinic granuloma
- Albinism
- Albinoidism
- Anemia
- Anetoderma
- Burns
- Chediak-higashi disease
- Cole disease
- Dermatomyositis
- Dyskeratosis congenita
- Elejalde syndrome
- Griscelli syndrome
- Idiopathic guttate hypomelanosis
- Incontinentia pigmenti
- Ito syndrome
- Lepromatous leprosy
- Leprosy
- Lymphoproliferative diseases
- Malassezia furfur
- Malignant melanoma
- Melanocortin 1 receptor mutations
- Melanoma
- Neuroectodermal melanolysosomal disease
- Nevus anemicus
- Nevus depigmentosus
- Oculo-cutaneous albinism
- Pinta
- Poikiloderma
- Proopiomelanocortin deficiency
- Psoriasis
- Reticulate acropigmentation of dohi
- Rothmund-thomson syndrome
- Skin damage
- Tinea versicolor
- Transient bullous dermolysis of the newborn
- Tuberculoid leprosy
- Vitiligo
Causes by Organ System
- Actinic granuloma
- Addison’s disease
- Albinism
- Albinoidism
- Anemia
- Anetoderma
- Angelman syndrome
- Azelaic acid
- Burns
- Candidiasis
- Chediak-higashi disease
- Cole disease
- Congenital
- Corticosteroid injection
- Cowden’s syndrome
- Cross-mckusick-breen syndrome
- Cutaneous t-cell lymphoma
- Deafness
- Dermatomyositis
- Diabetes mellitus
- Drugs
- Dysgammaglobulinemia
- Dyskeratosis congenita
- Elejalde syndrome
- Gastric carcinoma
- Genetic defects
- Griscelli syndrome
- Hashimoto’s thyroiditis
- Hirschsprung disease
- Homocystinuria
- Hydroquinone
- Hyperthyroidism
- Hypoparathyroidism
- Hypothyroidism
- Idiopathic guttate hypomelanosis
- Incontinentia pigmenti
- Infection
- Inflammation
- Ito syndrome
- Juvenile rheumatoid arthritis
- Kwashiorkor
- Lepromatous leprosy
- Leprosy
- Lymphoproliferative diseases
- Malassezia furfur
- Malignant melanoma
- Marasmus
- Melanocortin 1 receptor mutations
- Melanoma
- Menkes disease
- Mequinol
- Myasthenia gravis
- Nephropathic early-onset cystinosis
- Neuroectodermal melanolysosomal disease
- Nevus anemicus
- Nevus depigmentosus
- Oculo-cutaneous albinism
- Onchocerciasis
- Pazopanib
- Pernicious anemia
- Phenylketonuria
- Piebaldism
- Pinta
- Pituitary insufficiency
- Pityriasis alba
- Poikiloderma
- Polyendocrine deficiency syndrome type 2
- Proopiomelanocortin deficiency
- Pseudoatrophoderma colli
- Psoriasis
- Reticulate acropigmentation of dohi
- Rheumatoid arthritis
- Rothmund-thomson syndrome
- Sarcoidosis
- Scleroderma
- Secondary syphilis
- Skin damage
- Spondylometaphyseal dysplasia with combined immunodeficiency
- Syringomyelia
- Systemic lupus erythematosus
- Thrombopenia
- Tietz syndrome
- Tinea versicolor
- Transient bullous dermolysis of the newborn
- Trichorhinophalangeal syndrome type i
- Triploid syndrome
- Tuberculoid leprosy
- Tuberous sclerosis
- Varicosis
- Vitiligo
- Vogt-koyanagi-harada syndrome
- Waardenburg syndrome
- Whitaker syndrome
- Yemenite deaf-blind hypopigmentation syndrome
References
References
Editor-In-Chief: Template:Search infobox C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Luke Rusowicz-Orazem, B.S.
