Category:Disturbances of human pigmentation
Disturbances of human pigmentation, either loss or reduction, may be related to loss of melanocytes or the inability of melanocytes to produce melanin or transport melanosomes correctly.
Subcategories
This category has only the following subcategory.
A
Pages in category "Disturbances of human pigmentation"
The following 119 pages are in this category, out of 119 total. This list may not reflect recent changes.
A
- ABCD syndrome
- Acromelanism
- Albinism – black lock – cell migration disorder of the neurocytes of the gut – deafness syndrome
- Albinism in humans
- Albinism–black lock–cell migration disorder of the neurocytes of the gut–deafness syndrome
- Albinism–deafness syndrome
- Alezzandrini syndrome
- Argyria
- Arsenic poisoning
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F
G
H
L
M
P
- Pallister–Killian syndrome
- Partial albinism with immunodeficiency
- Partington amyloidosis
- Partington cutaneous amyloidosis
- Partington syndrome type II
- Pegum syndrome
- Periorbital hyperpigmentation
- Peutz–Jeghers syndrome
- Photoleukomelanodermatitis of Kobori
- Phylloid hypomelanosis
- Piebaldism
- Pigmentatio reticularis faciei et colli
- Pityriasis alba
- Poikiloderma
- Poikiloderma of Civatte
- Poikiloderma vasculare atrophicans
- Postinflammatory hypermelanosis
- Postinflammatory hyperpigmentation
- Postinflammatory hypopigmentation
- Progressive macular hypomelanosis