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A child that has prepubertal hypertrichosis. While hypertrichosis affects men and women equally, hypertrichosis of the ears, hypertrichosis of the nose, and hereditary hypertrichosis primarily affect males. [2] Prepubertal hypertrichosis can be present at birth or develop later on during childhood. [5]
"Nevus" is sometimes spelled "naevus" and "sebaceous" may also be spelled "sebaceus". "Epidermal nevus syndrome" is sometimes used as a synonym, but more often as a broader term referring to Schimmelpenning syndrome in addition to nevus comedonicus syndrome, CHILD syndrome, Becker's nevus syndrome, and phakomatosis pigmentokeratotica. [3]
The onset is in infancy. The skin lesions occur on cheeks, nose, fingers, toes and soles. [2] They may vary in appearance but frequently develop into non-healing ulcers. Interstitial lung disease is also common. Some individuals may not experience any obvious skin issues. All affected children fail to thrive. [citation needed]
Congenital melanocytic nevi may be divided into the following types: [6]: 690–1 Small-sized congenital melanocytic nevus is defined as having a diameter less than 2 cm (0.79 in). [6]: 690 Medium-sized congenital melanocytic nevus is defined as having a diameter more than 2 cm (0.79 in) but less than 20 cm (7.9 in). [6]: 690
Cutis marmorata telangiectatica congenita (CMTC) is a rare congenital vascular disorder that usually manifests in affecting the blood vessels of the skin. The condition was first recognized and described in 1922 by Cato van Lohuizen, [2] a Dutch pediatrician whose name was later adopted in the other common name used to describe the condition – Van Lohuizen syndrome.
Epidermal nevus syndrome, also known as Feuerstein and Mims syndrome, [1] [2] and Solomon's syndrome [1]: 775 [3] is a rare disease that was first described in 1968 and consists of extensive epidermal nevi with abnormalities of the central nervous system (CNS), skeleton, skin, cardiovascular system, genitourinary system and eyes.
The features include: 1) two or more clinically atypical nevi, 2) more than 100 nevi in patients between 20 and 50 years of age, 3) more than 50 nevi in patients under 20 years of age or more than 50 years of age, 4) more than one nevus in buttocks or instep, 5) nevi on the anterior scalp, 6) one or more pigmented lesions in the iris.
This skin lesion is quite common in the population, and it can present at birth, known as a congenital meloncytic nevus, or later in life as an acquired nevus. Should the nevi appear in toddler- or school-aged children, they are more likely to remain present throughout the rest of that person's life. [4]