Papular mucinosis of infancy

Papular mucinosis of infancy
Other names	Cutaneous mucinosis of infancy
Specialty	Dermatology

Papular mucinosis of infancy is a skin condition caused by fibroblasts producing abnormally large amounts of mucopolysaccharides, characterized by skin-colored or translucent papules.[1]^:186[2]

References

James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.

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[Andrews-1] James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.

[Bolognia-2] Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.

Mucinosis/Lichen myxedematosus
Localized lichen myxedematosus	Discrete papular lichen myxedematosus Acral persistent papular mucinosis Self-healing papular mucinosis/Self-healing juvenile cutaneous mucinosis Papular mucinosis of infancy Atypical lichen myxedematosus Atypical tuberous myxedema Nodular lichen myxedematosus
Other primary mucinoses	Cutaneous focal mucinosis Cutaneous lupus mucinosis Eccrine mucinosis Alopecia mucinosa Perifollicular mucinosis Stiff skin syndrome Generalized lichen myxedematosus
Secondary mucinoses	Basal-cell carcinoma Granuloma annulare

Papular mucinosis of infancy

See also

References