eMedicine Specialties > Dermatology > Diseases of Pigmentation
Albinism: Follow-up
Updated: Oct 30, 2009
Follow-up
Further Outpatient Care
- Patients with oculocutaneous albinism should be frequently screened for skin cancer.
- Patients with Chediak-Higashi syndrome, Hermansky-Pudlak syndrome, and Griscelli syndrome should be routinely monitored for advancement of the nonpigmentary disorders.
Complications
- Complications of oculocutaneous albinism type 1 include photophobia, severe-to-moderate reduced visual acuity, and nystagmus. The ocular complications in oculocutaneous albinism type 2, oculocutaneous albinism type 3, and oculocutaneous albinism type 4 are similar to those in oculocutaneous albinism type 1, but, in oculocutaneous albinism type 3, they are not as severe.
- Complications of Chediak-Higashi syndrome include easy bruising, mucosal bleeding, epistaxis and petechiae, recurrent infections primarily involving the respiratory system, and neutropenia. In the accelerated phase, fever; anemia; neutropenia; and, occasionally, thrombocytopenia, hepatosplenomegaly, lymphadenopathy, and jaundice may occur. Neurologic problems in Chediak-Higashi syndrome may include a peripheral and cranial neuropathy, autonomic dysfunction, weakness and sensory deficits, loss of deep tendon reflexes, clumsiness with a wide-based gait, seizures, and decreased motor nerve conduction velocities.
- Long-term complications of Hermansky-Pudlak syndrome include pulmonary fibrosis, granulomatous colitis, gingivitis, and kidney failure.
Patient Education
- Patients should use broad-spectrum sunscreens and should wear appropriate clothing to prevent ultraviolet-induced damage to the skin. Visual impairment can be improved by using corrective lenses.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous Chief Editor, William D. James, MD, to the development and writing of this article.
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References
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Further Reading
Keywords
albinism, albino, oculocutaneous albinism, oculocutaneous albinism type 1, oculocutaneous albinism type 2, oculocutaneous albinism type 3, oculocutaneous albinism type 4, OCA, OCA type 1, OCA type 2, OCA type 3, OCA type 4, ocular albinism, OA, Chediak-Higashi syndrome, CHS, Hermansky-Pudlak syndrome, HPS, Griscelli Syndrome, GS, congenital hypopigmentary disease
Follow-up: Albinism