Related Experiment Video
Updated: Jun 26, 2026

10:27
Recognition of Epidermal Transglutaminase by IgA and Tissue Transglutaminase 2 Antibodies in a Rare Case of Rhesus Dermatitis
Published on: December 15, 2011
Harlequin icthyosis: report of one case
Roopa Malik1, Viral Kumar, Meenakshi Chauhan
1PGIMS, Rohtak, Haryana, India. drroopa.sangwan@gmail.com
Archives of Gynecology and Obstetrics
|January 27, 2009
Abstract:
Harlequin icthyosis is a rare extremely severe autosomal recessive dermatosis. The appearance of newborn can be shocking to parents and health care providers. Prenatal diagnosis is possible only with great suspicion and can often be missed. To our knowledge only 100 cases have been reported so far, we report one case of harlequin icthyosis.
Related Concept Videos
Pleiotropy
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
Leishmaniasis
Leishmaniasis is a protozoal disease caused by species of the genus Leishmania and transmitted through the bite of infected female sandflies. The parasite exists in two principal morphological forms during its life cycle. A sandfly acquires intracellular amastigotes from an infected reservoir host, such as a dog. Within the sandfly, these forms differentiate into motile, flagellated promastigotes. During a subsequent blood meal, promastigotes are injected into the human host, where they...