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Primary milia: This common form of milia affects children and adults and can be found on the face or body, most commonly around the eyes, on the cheeks, and on the genital area.
Absence of fingerprints-congenital milia syndrome, also known simply as Baird syndrome is an extremely rare autosomal dominant genetic disorder which is characterized by a lack of fingerprints and the appearance of blisters and facial milia soon after birth. [2] It has been described in ten families worldwide. [3] [4]
Milia-like calcinosis is a cutaneous condition characterized by small, milia-like lesions that develop on the dorsal surface of the hands and the face. [1] See also
Miliaria, commonly known as heat rash, sweat rash, or prickly heat, [1] is a skin disease marked by small, itchy rashes due to sweat trapped under the skin by clogged sweat-gland ducts. Miliaria is a common ailment in hot and humid conditions, such as in the tropics and during the summer. [ 2 ]
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One study found that men with moderate-to-high levels of exhaustion had a 2.7-fold increased risk of heart attack within five years and a 2.25 higher risk within ten years. The study also found a ...
EVHC may occur randomly, or it can be inherited as an autosomal dominant trait; sporadic cases usually appear at 4–18 years of age. The cysts appear similar clinically to steatocystoma multiplex, as well as acneiform eruptions and milia. Histopathology is the basis of diagnosis. Retinoids, surgery, and lasers are used as treatment modalities.
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