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Trichorrhexis nodosa secondary to argininosuccinicaciduria

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Argininosuccinicaciduria is a rare metabolic disorder of the urea cycle associated with the inability to excrete nitrogenous waste in the form of urea. Along with low serum arginine, hepatomegaly, and mental retardation, congenital trichorrhexis nodosa is a distinguishing feature of the disorder. We present a 3.5-year-old girl diagnosed with argininosuccinicaciduria who presented to the dermatology clinic with hair thinning and loss since birth. Microscopic evaluation revealed nodular swellings on the hair shafts and frayed cortical fibers consistent with the diagnosis of trichorrhexis nodosa occurring in the setting of argininosuccinicaciduria.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 25-27 (3 pages)

Journal (Volume, Issue Number)

Pediatric dermatology (Volume 24, Issue 1)

Publication milestones

  • Published - 01/2007

Publication status

Published - 01/2007

ISSN

0736-8046

Publication IDs

  • Scopus: 33846960155
  • PubMed: 17300644

Publication metrics

Metrics

Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1
Scopus
citations
SciVal
FWCI
0.36
SciVal
Author count
3
SciVal
citations
22
SciVal
Paper percentile
75

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12
Citation count
39