Ophthalmic Features of Schopf-Schulz-Passarge Syndrome
Schopf–Schulz–Passarge syndrome (SSPS) is an ectodermal dysplasia of autosomal recessive inheritance. The SSPS involves two or more of the following structures: sweat glands, hair, teeth, nails, and other ectodermal structures. The features of this syndrome constitute multiple periocular and eyelid...
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| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2019-07-01
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| Series: | Delhi Journal of Ophthalmology |
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| Online Access: | https://journals.lww.com/10.7869/djo.487 |
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| author | Manpreet Singh Manpreet Kaur Aditi Mehta Grewal Zoramthara Zadeng Pankaj Gupta |
| author_facet | Manpreet Singh Manpreet Kaur Aditi Mehta Grewal Zoramthara Zadeng Pankaj Gupta |
| author_sort | Manpreet Singh |
| collection | DOAJ |
| description | Schopf–Schulz–Passarge syndrome (SSPS) is an ectodermal dysplasia of autosomal recessive inheritance. The SSPS involves two or more of the following structures: sweat glands, hair, teeth, nails, and other ectodermal structures. The features of this syndrome constitute multiple periocular and eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypodontia, hypotrichosis, and nail dystrophy. We present pictorial description of the SSPS. |
| format | Article |
| id | doaj-art-080482b30e8446bc88b30d5af7d2ba4d |
| institution | OA Journals |
| issn | 0972-0200 2454-2784 |
| language | English |
| publishDate | 2019-07-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Delhi Journal of Ophthalmology |
| spelling | doaj-art-080482b30e8446bc88b30d5af7d2ba4d2025-08-20T02:10:57ZengWolters Kluwer Medknow PublicationsDelhi Journal of Ophthalmology0972-02002454-27842019-07-01301686910.7869/djo.487Ophthalmic Features of Schopf-Schulz-Passarge SyndromeManpreet SinghManpreet KaurAditi Mehta GrewalZoramthara ZadengPankaj GuptaSchopf–Schulz–Passarge syndrome (SSPS) is an ectodermal dysplasia of autosomal recessive inheritance. The SSPS involves two or more of the following structures: sweat glands, hair, teeth, nails, and other ectodermal structures. The features of this syndrome constitute multiple periocular and eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypodontia, hypotrichosis, and nail dystrophy. We present pictorial description of the SSPS.https://journals.lww.com/10.7869/djo.487eccrine hidrocystoma of eyelideyelid translucent cystsapocrine hidrocystomasschopf-schulz-passarge syndrome |
| spellingShingle | Manpreet Singh Manpreet Kaur Aditi Mehta Grewal Zoramthara Zadeng Pankaj Gupta Ophthalmic Features of Schopf-Schulz-Passarge Syndrome Delhi Journal of Ophthalmology eccrine hidrocystoma of eyelid eyelid translucent cysts apocrine hidrocystomas schopf-schulz-passarge syndrome |
| title | Ophthalmic Features of Schopf-Schulz-Passarge Syndrome |
| title_full | Ophthalmic Features of Schopf-Schulz-Passarge Syndrome |
| title_fullStr | Ophthalmic Features of Schopf-Schulz-Passarge Syndrome |
| title_full_unstemmed | Ophthalmic Features of Schopf-Schulz-Passarge Syndrome |
| title_short | Ophthalmic Features of Schopf-Schulz-Passarge Syndrome |
| title_sort | ophthalmic features of schopf schulz passarge syndrome |
| topic | eccrine hidrocystoma of eyelid eyelid translucent cysts apocrine hidrocystomas schopf-schulz-passarge syndrome |
| url | https://journals.lww.com/10.7869/djo.487 |
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