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Pigmentation Disorders |11029|
Pigmentation Disorders Subsets
Hypopigmentations
Hyperpigmentations
Westerhof Beemer Cormane Syndrome
Cafe-au-Lait Spots Syndrome
Argyria
Urticaria Pigmentosa
See Also ↔
 
 
“Pigmentation Disorders”  
  In and on our body's integumentary system, Pigmentation Disorders are skin dis-orders (cutaneous conditions) involving the pigment of the skin. *
[11930]
“Xeroderma Pigmentosum”  
  In our body's integumentary system, the DNA repair-deficiency dis-order, Xeroderma Pigmentosum is a skin abnormality including photosensitivities, indicative to a specific set of signs, symptoms or other health indicators, associated as a pigmentation dis-order, a preneoplastic condition, and genetic skin conditions. **
[13747]
“Cafe Au Lait Spots Syndrome”  

Cafe-au-Lait Spots Syndrome

  In our body, the pigmentation dis-order, Cafe Au Lait Spots Syndrome is a skin manifestation of light brown pigmented macules, indicative to a specific set of signs, symptoms or other health indicators, associated with the health challenges of neurofibromatosis, Watson syndrome, and Albright's syndrome. **
[13802]
“Argyria”  
  Inand on our body's skin, the pigmentation dis-order, Argyria is a poisoning, indicative to a specific set of signs, symptoms or other health indicators, associated with a health challenge caused by prolonged use of silver salts.
  Inand on our body's skin, the dis-order, Argyria is a permanent ashen-gray discoloration of the skin, conjunctiva, and internal organs resulting from long-continued exposure to salts of silver. **
[14018]
“Incontinentia Pigmenti (Bloch-Sulzberger Syndrome)”  

Hypomelanosis of Ito

  In our body, the genodermatosis pigmentation dis-order, Incontinentia Pigmenti (Hypomelanosis of Ito) is a phakomatosis genetic skin dis-order indicative to a specific set of signs, symptoms or other health indicators, associated with a skin abnormality manifesting usually as a multiple system abnormality.

Incontinentia Pigmenti

  In our body, the Incontinentia Pigmenti occurring mostly in females and characterized by skin changes in three phases; the vesiculobullous, verrucous papillomatous, and macular melanodermic, associated as a neuro-cutaneous health challenge. **
[14771]
“Yellow Nail Syndrome”  
  In and on our body's integumentary system, the pigmentation dis-order, Yellow Nail Syndrome is a rare condition characterized by the presence of yellow nails, lymphedema, and/or pleural effusion with respiratory tract involvement, associated with a health challenge. **
[18058]
References & Citations:
1. Westerveld A. et al "Molecular cloning of a human DNA repair gene"   Nature. 1984 Aug 2-8;310(5976):425-9  
2. Jaspers NG. et al "First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure"   Am J Hum Genet. 2007 Mar;80(3):457-66  
3. Khan I. et al "Impact of age-associated cyclopurine lesions on DNA repair helicases"   PLoS One. 2014 Nov 19;9(11):e113293  
4. Landy SJ. et al "Incontinentia pigmenti (Bloch-Sulzberger syndrome)"   J Med Genet. 1993 Jan;30(1):53-9  
 
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