eMedicine Specialties > Dermatology > Diseases of Pigmentation
Hypomelanosis of Ito: Treatment & Medication
Updated: Aug 31, 2009
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Treatment
Medical Care
- No treatment is administered for the cutaneous findings of hypomelanosis of Ito (HI).
- Cover-up makeup can be used if the patient desires it.
- Associated diseases, including the following, require appropriate specialty care:
- Seizures
- Mental retardation
- Hearing abnormalities
- Tooth deformities
- Visual problems
- Orthopedic problems
- Diagnosis is important to guide genetic counseling.
Surgical Care
- No surgical treatment is required for the cutaneous problems.
- Consult a surgeon in regard to the associated surgical problems, as the physical examination findings indicate.
Consultations
- Consult a genetic counselor.
- Consult a neurologist, psychiatrist, orthopedic specialist, dentist, or ophthalmologist, as the features of the history and physical examination indicate.
Activity
No limitations on activity are required.
More on Hypomelanosis of Ito |
| Overview: Hypomelanosis of Ito |
| Differential Diagnoses & Workup: Hypomelanosis of Ito |
Treatment & Medication: Hypomelanosis of Ito |
| Follow-up: Hypomelanosis of Ito |
| Multimedia: Hypomelanosis of Ito |
| References |
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References
Nehal KS, PeBenito R, Orlow SJ. Analysis of 54 cases of hypopigmentation and hyperpigmentation along the lines of Blaschko. Arch Dermatol. Oct 1996;132(10):1167-70. [Medline].
Gupta S, Shah S, Mcgaw A, Mercado T, Zaslav AL, Tegay D. Trisomy 2 mosaicism in hypomelanosis of Ito. Am J Med Genet A. Oct 15 2007;143A(20):2466-8. [Medline].
McKusic VA. Online Mendelian Inheritance in Man (OMIM) [serial online]. 2000;Available at: http://w3.ncbi.nlm.nih.gov/Omim/. [Full Text].
Scott A, Micallef C, Hale SL, Watts P. Cortical visual impairment in hypomelanosis of Ito. J Pediatr Ophthalmol Strabismus. Jul-Aug 2008;45(4):240-1. [Medline].
Iype M, Iype T, Geetha S, Retnakumar J. Hypomelanosis of Ito with cerebral malformation. Indian J Pediatr. Nov 2007;74(11):1044-5. [Medline].
Vergine G, Mencarelli F, Diomedi-Camassei F, et al. Glomerulocystic kidney disease in hypomelanosis of Ito. Pediatr Nephrol. Jul 2008;23(7):1183-7. [Medline].
Donnai D, Read AP, McKeown C, Andrews T. Hypomelanosis of Ito: a manifestation of mosaicism or chimerism. J Med Genet. Dec 1988;25(12):809-18. [Medline].
Fritz B, Kuster W, Orstavik KH, Naumova A, Spranger J, Rehder H. Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of Xp. Hum Genet. Oct 1998;103(4):441-9. [Medline].
Glover MT, Brett EM, Atherton DJ. Hypomelanosis of Ito: spectrum of the disease. J Pediatr. Jul 1989;115(1):75-80. [Medline].
Hatchwell E. Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis. J Med Genet. Mar 1996;33(3):177-83. [Medline].
Pascual-Castroviejo I, Roche C, Martinez-Bermejo A, et al. Hypomelanosis of ITO. A study of 76 infantile cases. Brain Dev. Jan 1998;20(1):36-43. [Medline].
Further Reading
Keywords
hypomelanosis of Ito, HI, incontinentia pigmenti achromians, hypopigmented whorls of skin along Blaschko lines
Treatment & Medication: Hypomelanosis of Ito