"Ichthyosis, X-Linked" 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.
Chronic form of ichthyosis that is inherited as a sex-linked recessive trait carried on the X-chromosome and transmitted to the male offspring. It is characterized by severe scaling, especially on the extremities, and is associated with steroid sulfatase deficiency.
| Descriptor ID |
D016114
|
| MeSH Number(s) |
C16.131.831.512.420 C16.320.322.241 C16.320.565.925.400 C16.320.850.408 C16.614.492.420 C17.800.428.333.420 C17.800.804.512.420 C17.800.827.408 C18.452.648.925.400
|
| Concept/Terms |
Ichthyosis, X-Linked- Ichthyosis, X-Linked
- Ichthyoses, X-Linked
- Ichthyosis, X Linked
- Ichthyosis, Sex-Linked
- Ichthyoses, Sex-Linked
- Ichthyosis, Sex Linked
Placental Steroid Sulfatase Deficiency- Placental Steroid Sulfatase Deficiency
- Steroid Sulfatase Deficiency
- Deficiencies, Steroid Sulfatase
- Deficiency, Steroid Sulfatase
- Steroid Sulfatase Deficiencies
- Sulfatase Deficiencies, Steroid
- Sulfatase Deficiency, Steroid
|
Below are MeSH descriptors whose meaning is more general than "Ichthyosis, X-Linked".
- Diseases [C]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
- Skin Abnormalities [C16.131.831]
- Ichthyosis [C16.131.831.512]
- Ichthyosis, X-Linked [C16.131.831.512.420]
- Genetic Diseases, Inborn [C16.320]
- Genetic Diseases, X-Linked [C16.320.322]
- Ichthyosis, X-Linked [C16.320.322.241]
- Metabolism, Inborn Errors [C16.320.565]
- Steroid Metabolism, Inborn Errors [C16.320.565.925]
- Ichthyosis, X-Linked [C16.320.565.925.400]
- Skin Diseases, Genetic [C16.320.850]
- Ichthyosis, X-Linked [C16.320.850.408]
- Infant, Newborn, Diseases [C16.614]
- Ichthyosis [C16.614.492]
- Ichthyosis, X-Linked [C16.614.492.420]
- Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
- Keratosis [C17.800.428]
- Ichthyosis [C17.800.428.333]
- Ichthyosis, X-Linked [C17.800.428.333.420]
- Skin Abnormalities [C17.800.804]
- Ichthyosis [C17.800.804.512]
- Ichthyosis, X-Linked [C17.800.804.512.420]
- Skin Diseases, Genetic [C17.800.827]
- Ichthyosis, X-Linked [C17.800.827.408]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Metabolism, Inborn Errors [C18.452.648]
- Steroid Metabolism, Inborn Errors [C18.452.648.925]
- Ichthyosis, X-Linked [C18.452.648.925.400]
Below are MeSH descriptors whose meaning is more specific than "Ichthyosis, X-Linked".
This graph shows the total number of publications written about "Ichthyosis, X-Linked" by people in this website by year, and whether "Ichthyosis, X-Linked" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Ichthyosis, X-Linked" by people in Profiles.
-
Banding pattern on polarized hair microscopic examination and unilateral polymicrogyria in a patient with steroid sulfatase deficiency. Arch Dermatol. 2012 Jan; 148(1):73-8.
-
Clinical pathologic correlation of superficial corneal opacities in X-linked ichthyosis. Am J Ophthalmol. 1994 Oct 15; 118(4):477-84.