"Acrodermatitis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Inflammation involving the skin of the extremities, especially the hands and feet. Several forms are known, some idiopathic and some hereditary. The infantile form is called Gianotti-Crosti syndrome.
| Descriptor ID |
D000169
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| MeSH Number(s) |
C16.131.831.066 C17.800.174.100 C17.800.804.066
|
| Concept/Terms |
Gianotti-Crosti Syndrome- Gianotti-Crosti Syndrome
- Gianotti Crosti Syndrome
- Syndrome, Gianotti-Crosti
- Acropapulo-Vesicular Syndrome
- Acropapulo Vesicular Syndrome
- Acropapulo-Vesicular Syndromes
- Syndrome, Acropapulo-Vesicular
- Syndromes, Acropapulo-Vesicular
- Papulovesicular Acrolocated Syndrome
- Papulovesicular Acrolocated Syndromes
- Syndromes, Papulovesicular Acrolocated
- Infantile Papular Acrodermatitis
- Infantile Papular Acrodermatitides
- Papular Acrodermatitides, Infantile
- Papular Acrodermatitis, Infantile
- Papular Acrodermatitis of Childhood
- Childhood Papular Acrodermatitides
- Childhood Papular Acrodermatitis
- Acrodermatitis Papulosa Infantum
- Acrodermatitis Papulosa Infantums
- Erythemato-Vesiculo-Papulous Eruptive Syndrome
- Erythemato Vesiculo Papulous Eruptive Syndrome
- Erythemato-Vesiculo-Papulous Eruptive Syndromes
- Syndrome, Erythemato-Vesiculo-Papulous Eruptive
- Syndromes, Erythemato-Vesiculo-Papulous Eruptive
|
Below are MeSH descriptors whose meaning is more general than "Acrodermatitis".
Below are MeSH descriptors whose meaning is more specific than "Acrodermatitis".
This graph shows the total number of publications written about "Acrodermatitis" by people in this website by year, and whether "Acrodermatitis" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 3 | 0 | 3 |
| 2002 | 1 | 0 | 1 |
| 2005 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Acrodermatitis" by people in Profiles.
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Vahidnezhad H, Youssefian L, Sotoudeh S, Liu L, Guy A, Lovell PA, Kariminejad A, Zeinali S, McGrath JA, Uitto J. Genomics-based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica. Hum Mutat. 2020 05; 41(5):906-912.
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Atanasovski M, Dele-Michael A, Dasgeb B, Ganger L, Mehregan D. A case report of Gianotti-Crosti post vaccination with MMR and dTaP. Int J Dermatol. 2011 May; 50(5):609-10.
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Chew AL, Chan I, McGrath JA, Atherton DJ. Infantile acquired zinc deficiency resembling acrodermatitis enteropathica. Clin Exp Dermatol. 2005 Sep; 30(5):594-5.
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Nakano A, Nakano H, Hanada K, Nomura K, Uitto J. ZNT4 gene is not responsible for acrodermatitis enteropathica in Japanese families. Hum Genet. 2002 Feb; 110(2):201-2.
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Bleck O, Ashton GH, Mallipeddi R, South AP, Whittock NV, McLean WH, Atherton DJ, McGrath JA. Genomic localization, organization and amplification of the human zinc transporter protein gene, ZNT4, and exclusion as a candidate gene in different clinical variants of acrodermatitis enteropathica. Arch Dermatol Res. 2001 Aug; 293(8):392-6.
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Bleck O, McGrath JA, South AP. Searching for candidate genes in the new millennium. Clin Exp Dermatol. 2001 May; 26(3):279-83.
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Gluckman SJ, Heyman W. Diagnosis: acrodermatitis continua of Hallopeau. Clin Infect Dis. 2001 Feb 01; 32(3):431, 505.