Hypomelanosis: Difference between revisions
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===Causes in Alphabetical Order<ref>Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:77 ISBN 1591032016</ref> <ref>Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:68 ISBN 140510368X</ref>=== | ===Causes in Alphabetical Order<ref>Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:77 ISBN 1591032016</ref> <ref>Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:68 ISBN 140510368X</ref>=== | ||
{{columns-list | {{columns-list| | ||
*[[Actinic granuloma]] | *[[Actinic granuloma]] | ||
*[[Addison's disease]] | *[[Addison's disease]] |
Latest revision as of 21:21, 10 January 2020
Hypomelanosis |
Template:Search infobox Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Luke Rusowicz-Orazem, B.S.
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
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
Causes in Alphabetical Order[1] [2]
- 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
See Also