books pigmentation disorders
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# Human pigmentation disorders
# Skin pigmentation disorders
# skin pigmentation
# pigmentation treatment
# Removing pigmentation marks on the skin
# Pigmentation removal
# pigmentation in plants
# silver pigmentation
# hypopigmentation
# Hyperpigmentation
# Prevention of teeth stains and pigmentation
# Tips to prevent lip pigmentation
# teeth pigmentation
# Prevention of pigmentation and discoloration of the skin
# Reduce skin pigmentation
# Causes of skin pigmentation
# Causes of pigmentation around the mouth
# What is the treatment for facial pigmentation?
# What is the cause of facial pigmentation?
# What are mental disorders?
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Source: wikipedia.org
اضطرابات التصبغ (Info)
Disturbances of human pigmentation، either loss or reduction، may be related to loss of خلية ميلانينيةs or the inability of melanocytes to produce ميلانين or transport جسيم ميلانينيs correctly.
- Albinism–black lock–cell migration disorder of the neurocytes of the gut–deafness syndrome (ABCD syndrome)
- Albinism–deafness syndrome (Woolf syndrome، Ziprkowski–Margolis syndrome)
- Alezzandrini syndrome
- تفضض
- تسمم بالزرنيخ
- Berlin syndrome
- Canthaxanthin
- متلازمة شدياق-هيغاشي
- Chrysiasis
- Cross–McKusick–Breen syndrome (Cross syndrome، oculocerebral-hypopigmentation syndrome)
- Dermatopathia pigmentosa reticularis (dermatopathia pigmentosa reticularis hyperkeratotica et mutilans، dermatopathia pigmentosa reticularis hypohidotica et atrophica، dermatopathic pigmentosa reticularis)
- Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi، symmetrical dyschromatosis of the extremities)
- Dyschromatosis universalis hereditaria
- متلازمة إليخالدي (Griscelli syndrome type 1)
- Familial progressive hyperpigmentation
- Galli–Galli disease
- Griscelli syndrome type 2 (partial albinism with immunodeficiency)
- Griscelli syndrome type 3
- اكتناز الحديد (bronze diabetes)
- Hemosiderin hyperpigmentation
- متلازمة هيرمانسكي-بودلاك
- Idiopathic guttate hypomelanosis (leukopathia symmetrica progressiva)
- Iron metallic discoloration
- متلازمة واردينبيرغ
- تسمم بالرصاص
- الوضح
- Melanoma-associated leukoderma
- كلف (chloasma faciei، mask of pregnancy)
- متلازمة موكميل
- Necklace of Venus
- Nevus anemicus
- وحمة زائلة الصباغ
- مهق عيني
- Oculocutaneous albinism
- متلازمة باليستر-كيليان
- Periorbital hyperpigmentation
- Photoleukomelanodermatitis of Kobori
- Phylloid hypomelanosis
- لمع
- Pigmentatio reticularis faciei et colli
- النخالية ألبا
- Poikiloderma of Civatte
- Poikiloderma vasculare atrophicans
- فرط التصبغ (postinflammatory hypermelanosis)
- Postinflammatory hypopigmentation
- Progressive macular hypomelanosis
- بهاق رباعي الألوان
- Reticular pigmented anomaly of the flexures (dark dot disease، Dowling–Degos" disease)
- Reticulate acropigmentation of Kitamura
- Revesz syndrome
- Riehl melanosis
- Scratch dermatitis (flagellate pigmentation from bleomycin)
- بهاق مقطعي
- متلازمة واردينبيرغ
- Shiitake mushroom dermatitis (flagellate mushroom dermatitis، mushroom worker"s disease، shiitake-induced toxicoderma)
- Tar melanosis (melanodermatitis toxica lichenoides)
- Tietz syndrome
- Titanium metallic discoloration
- Transient neonatal pustular melanosis (transient neonatal pustulosis، lentigines neonatorum)
- بهاق ثلاثي الألوان
- Vagabond"s leukomelanoderma
- Vasospastic macule
- بهاق
- بهاق منقط
- مرض فوجت-كوياناجا-هارادا
- متلازمة واردينبيرغ
- Wende–Bauckus syndrome (Pegum syndrome)
- حلقة ورونوف
- X-linked reticulate pigmentary disorder (familial cutaneous amyloidosis، Partington amyloidosis، Partington cutaneous amyloidosis، Partington syndrome type II، reticulate pigmentary disorder، X-linked reticulate pigmentary disorder with systemic manifestations)
- Yemenite deaf-blind hypopigmentation syndrome
