Results 221 to 230 of about 19,470 (278)

A case report of extensive vitiligo. [PDF]

, 1997
Wee, T A
core  

A Rare Type of Bullous Disorder in a Child. Can It Be Chronic Bullous Disease of Childhood? [PDF]

Clin Case Rep
Yadav R, Poudel I, Poudyal Y, Chaudhary N.   +3 more
europepmc   +1 more source

Griscelli Syndrome in Two Siblings with Silvery Hair: A Case Report. [PDF]

JNMA J Nepal Med Assoc
Khwaja H, Rajan AR, Lingayat N, Dhasal S.   +3 more
europepmc   +1 more source

Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.

, 1989
Merlin G. Butler
openalex  

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Disorders of Hypopigmentation

Journal of drugs in dermatology : JDD, 2019
Hypopigmentation of the skin is frequently encountered in childhood. Such a presentation can be either congenital or acquired, and generalized or more localized. Considering that hypopigmentation can be an early indication of serious (congenital) conditions, a medical history and thorough clinical examination, including Wood's light investigation, is ...
Albert Wolkerstorfer
exaly   +4 more sources

Biology of hypopigmentation

Journal of the American Academy of Dermatology, 1988
A review of the basics of pigment cell biology is followed by a discussion of the characteristics of several disorders of hypopigmentation. By determining such features as inheritance pattern, time of onset (congenital, childhood, adulthood), natural history (stable vs progressive), type of pigment loss (diffuse or circumscribed), distribution of ...
J L, Bolognia, J M, Pawelek
openaire   +2 more sources

Postinflammatory hypopigmentation and hyperpigmentation

Seminars in Cutaneous Medicine and Surgery, 1997
Postinflammatory hypopigmentation and hyperpigmentation are frequently encountered problems and represent the sequelae of various cutaneous disorders as well as therapeutic interventions. However, the underlying mechanisms and the variability individuals show for developing hypopigmentation or hyperpigmentation are not well understood.
R, Ruiz-Maldonado, M L, Orozco-Covarrubias   +1 more
openaire   +2 more sources

Hypopigmentation in Angelman syndrome

American Journal of Medical Genetics, 1993
AbstractChromosome region 15q is thought to contain one or more genes that are important for melanin pigment synthesis in the hair, skin, and eyes. Hypopigmentation has been identified in the Prader‐Willi (PWS) and Angelman (AS) syndromes. We have examined 6 individuals with AS to further characterize the pigment pattern in this condition.
R A, King, G L, Wiesner, D, Townsend, J G, White   +3 more
openaire   +2 more sources