Oculocutaneous albinism

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Oculocutaneous albinism
Classification and external resources
Specialty endocrinology
ICD-10 E70.3
ICD-9-CM 270.2
OMIM 203100 203200 203290 606574
MeSH D016115
GeneReviews

Oculocutaneous albinism (OCA) is a form of albinism involving the eyes (oculo-), the skin (-cutaneous), and according to some definitions, the hair.[1] Overall, an estimated 1 in 20,000 people worldwide are born with oculocutaneous albinism.[2] OCA is caused by mutations in several genes that control the synthesis of melanin within the melanocytes.[3] Four types of oculocutaneous albinism have been described, all caused by a disruption of melanin synthesis and all autosomal recessive disorders.[4][5]:864

Types[edit]

Name OMIM Gene Description
OCA1 203100
606952
TYR OCA1 is caused by an alteration of the tyrosinase gene, and can occur in two variations. The first is OCA1a, and means that the organism cannot develop pigment at all.[6] The hair is usually white (often translucent) and the skin very pale. Vision usually ranges from 20/200 to 20/400. The second is OCA1b, which has several subtypes itself.[7] Some individuals with OCA1b can tan and also develop pigment in the hair.[8] One subtype of OCA1b is called OCA1b TS (temperature sensitive), where the tyrosinase can only function below a certain temperature, which causes the body hair in cooler body regions to develop pigment (i.e. get darker). (An equivalent mutation produces the coat pattern in Siamese cats.[9]) Another variant of OCA1b, called Albinism, yellow mutant type is more common among the Amish than in other populations, and results in blonde hair and the eventual development of skin pigmentation during infancy, though at birth is difficult to distinguish from other types.[7][10] About 1 in 40,000 people have some form of OCA1.[11]
OCA2 203200 OCA2 The most common type of albinism, is caused by mutation of the P gene. People with OCA2 generally have more pigment and better vision than those with OCA1, but cannot tan like some with OCA1b. A little pigment can develop in freckles or moles.[8] People with OCA2 usually have fair skin but often not as pale as OCA1, and pale blonde to golden, strawberry blonde, or even brown hair, and most commonly blue eyes. Affected people of African descent usually have a different phenotype (appearance): yellow hair, pale skin, and blue, gray or hazel eyes. About 1 in 15,000 people have OCA2.[12][11] The gene MC1R doesn't cause OCA2, but does affect its presentation.[1]
OCA3 203290 TYRP1 Has only been partially researched and documented. It is caused by mutation of the tyrosinase-related protein-1 (Tyrp1) gene. Cases have been reported in Africa and New Guinea. Affected individuals typically have red hair, reddish-brown skin and blue or gray eyes. Variants may include rufous oculocutaneous albinism (ROCA or xanthism). The incidence rate of OCA3 is unknown.[13][11]
OCA4 606574 SLC45A2 Is very rare outside Japan, where OCA4 accounts for 24% of albinism cases. OCA4 can only be distinguished from OCA2 through genetic testing, and is caused by mutation of this membrane-associated transporter protein (MATP) gene.[14][11] Several German patients were identified in 2004.[15]
OCA5 615312 OCA5 waas identified in a Pakistani family with "golden-colored hair, white skin, nystagmus, photophobia, foveal hypoplasia, and impaired visual acuity, regardless of their sex and age". Genetic analysis localized the defect to human chromosome region 4q24, but failed to identify a candidate gene.[16][17]
OCA6 113750 SLC24A5 One of the rarest forms of OCA, OCA6 was detected in Chinese individuals by is not thought to be limited to this ethnicity. It is heterogeneous in its effect of hair color, and results from mutations in the SLC24A5 gene, a membrane transported that plays a role in pigmentation in a range of vertebrate species.[17][18]
OCA7 615179 C10orf11 OCA7 was originally characterized in a family from the Faroe Islands, but was subsequently identified in a Lithuanian patent. It is characterized by lighter pigmentation, and significant effects on the eye, including decreased visual acuity and misrouting of neuronal tracks through the optic chiasm. It is due to mutation of a gene of unknown function, C10orf11 (11th uncharacterized open reading frame on chromosome 10, OMIM: 614537).[17][19]

See also[edit]

References[edit]

  1. ^ a b "Oculocutaneous albinism - Genetics Home Reference". 
  2. ^ http://ghr.nlm.nih.gov/condition/oculocutaneous-albinism
  3. ^ http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=55
  4. ^ Grønskov K, Ek J, Brondum-Nielsen K (2007). "Oculocutaneous albinism". Orphanet Journal of Rare Diseases. 2: 43. doi:10.1186/1750-1172-2-43. PMC 2211462Freely accessible. PMID 17980020. 
  5. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
  6. ^ OCA1A page at Online Mendelian Inheritance in Man Database, Johns Hopkins University
  7. ^ a b OCA1B page at Online Mendelian Inheritance in Man Database, Johns Hopkins University
  8. ^ a b "Facts about Albinism" (archived), by Dr. Richard King et al., 2009
  9. ^ Giebel LB, Tripathi RK, King RA, Spritz RA (March 1991). "A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse". The Journal of Clinical Investigation. 87 (3): 1119–22. doi:10.1172/JCI115075. PMC 329910Freely accessible. PMID 1900309. 
  10. ^ "Ocular Manifestations of Albinism", by Dr. Mohammed O. Peracha, at eMedicine, 13 September 2005; retrieved 31 March 2007
  11. ^ a b c d "Albinism", by Dr. Raymond E. Boissy, Dr. James J. Nordlund, et al., at eMedicine, 22 August 2005; retrieved 31 March 2007
  12. ^ OCA2 page at Online Mendelian Inheritance in Man Database, Johns Hopkins University
  13. ^ OCA3 page at Online Mendelian Inheritance in Man Database, Johns Hopkins University
  14. ^ OCA4 page at Online Mendelian Inheritance in Man Database, Johns Hopkins University
  15. ^ Rundshagen U, Zühlke C, Opitz S, Schwinger E, Käsmann-Kellner B (February 2004). "Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4". Human Mutation. 23 (2): 106–10. doi:10.1002/humu.10311. PMID 14722913. 
  16. ^ OCA5 page at Online Mendelian Inheritance in Man Database, Johns Hopkins University
  17. ^ a b c Montoliu L, Grønskov K, Wei A, Martínez-García M, Fernández A, Arveiler B, Morice-Picard F, Riazuddin S, Suzuki T, Ahmed Z, Rosenberg T, Li W (January 2014). "Increasing the complexity: new genes and new types of albinism". Pigment Cell & Melanoma Research. 27 (1): 11–18. doi:10.1111/pcmr.12167. PMID 24066960. 
  18. ^ SHEP4 page at Online Mendelian Inheritance in Man Database, Johns Hopkins University
  19. ^ OCA7 page at Online Mendelian Inheritance in Man Database, Johns Hopkins University

External links[edit]