:Griscelli syndrome type 3
{{Infobox medical condition (new)
| synonyms = Griscelli-Pruniéras syndrome type 3
| name = Griscelli syndrome type 3
| image = Autosomal recessive - en.svg
| alt =
| caption = This condition is inherited in an autosomal recessive manner.
| pronounce =
| field =
| geneReviewsID =
| symptoms =
| complications =
| onset =
| duration =
| types =
| causes =
| risks =
| diagnosis =
| differential =
| prevention =
| treatment =
| medication =
| prognosis =
| frequency =
| deaths =
}}
Griscelli syndrome type 3 is a disorder of melanosome transport presenting initially with hypopigmentation.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. {{ISBN|0-7216-2921-0}}.{{rp|866}}
See also
References
{{reflist}}
External links
{{Medical resources
| DiseasesDB =
| ICD10 = E70.3
| ICD9 =
| ICDO =
| OMIM = 609227
| MedlinePlus =
| eMedicineSubj =
| eMedicineTopic =
| MeshID = C537303
| GeneReviewsName =
| Orphanet = 79478
}}
{{Pigmentation disorders}}
Category:Disturbances of human pigmentation
{{Cutaneous-condition-stub}}