"Incontinentia Pigmenti" 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.
A genodermatosis occurring mostly in females and characterized by skin changes in three phases - vesiculobullous, verrucous papillomatous, and macular melanodermic. Hyperpigmentation is bizarre and irregular. Sixty percent of patients have abnormalities of eyes, teeth, central nervous system, and skin appendages.
Descriptor ID |
D007184
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MeSH Number(s) |
C16.131.077.445 C16.131.831.580 C16.320.850.420 C17.800.621.497 C17.800.804.580 C17.800.827.420
|
Concept/Terms |
Incontinentia Pigmenti- Incontinentia Pigmenti
- Bloch-Siemens-Sulzberger Syndrome
- Bloch-Siemens Syndrome
- Bloch-Sulzberger Syndrome
- Bloch Sulzberger Syndrome
- Syndrome, Bloch-Sulzberger
|
Below are MeSH descriptors whose meaning is more general than "Incontinentia Pigmenti".
Below are MeSH descriptors whose meaning is more specific than "Incontinentia Pigmenti".
This graph shows the total number of publications written about "Incontinentia Pigmenti" by people in this website by year, and whether "Incontinentia Pigmenti" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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2000 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
2019 | 1 | 0 | 1 |
2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Incontinentia Pigmenti" by people in Profiles.
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Interferon-ß Therapy in a Patient with Incontinentia Pigmenti and Autoantibodies against Type I IFNs Infected with SARS-CoV-2. J Clin Immunol. 2021 07; 41(5):931-933.
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Multicystic Dysplastic Kidney and Incontinentia Pigmenti: Coexistence of 2 Rare Diseases. Iran J Kidney Dis. 2019 Jan; 13(1):67-70.
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A female newborn with papulovesicular lesions. J Dtsch Dermatol Ges. 2018 Nov; 16(11):1383-1386.
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Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-?B activation and leads to incontinentia pigmenti. J Allergy Clin Immunol. 2017 Dec; 140(6):1671-1682.e2.
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A pregnancy following PGD for X-linked dominant [correction of X-linked autosomal dominant] incontinentia pigmenti (Bloch-Sulzberger syndrome): case report. Hum Reprod. 2000 Dec; 15(12):2650-2.