2001
DOI: 10.1007/bf02737867
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Alopecia areata universalis in an infant

Abstract: Alopecia areata should be included in the differential diagnosis of generalized alopecia presenting at or shortly after birth. For purposes of genetic counseling and prognosis, it is crucial that a correct diagnosis be made.

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Cited by 6 publications
(6 citation statements)
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“…Onychomadesis has been associated with alopecia areata. LaRow et al . published a case report of a 2‐year‐old child with alopecia areata universalis, and Tosti et al .…”
Section: Autoimmune Diseasementioning
confidence: 99%
“…Onychomadesis has been associated with alopecia areata. LaRow et al . published a case report of a 2‐year‐old child with alopecia areata universalis, and Tosti et al .…”
Section: Autoimmune Diseasementioning
confidence: 99%
“…In the latter, the lesions are well‐circumscribed patches of loss of hair (alopecia) 2–6 . Alopecia universalis, a variant of AA, 7 is a rather unusual expression and has sparingly been reported in the English literature 1 . The presence of generalized hair loss therefore in infants is important, and should conform to the diagnosis of AU, 8 as in the current case.…”
mentioning
confidence: 58%
“…Early onset of AU invariably has a poor prognosis. In the previous case report of infantile AU, the hair was lost within 2 months of birth and never regrew 1 . PUVA has been reported to be an effective and safe treatment for AA.…”
mentioning
confidence: 87%
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“…A younger age of onset is believed to predict a poorer prognosis. Very few occurrences of AA in infants less than 6 months of age have been described in the Western literature (4–9).…”
mentioning
confidence: 99%