Schöpf–Schulz–Passarge syndrome
This article will address the topic of Schöpf–Schulz–Passarge syndrome, which has gained relevance in recent years due to its impact on various aspects of society. From technological advances to changes in work dynamics, Schöpf–Schulz–Passarge syndrome has generated great interest and debate among experts and the general population. Along these lines, the influence of Schöpf–Schulz–Passarge syndrome in different contexts will be analyzed, as well as its short- and long-term implications. Future perspectives on Schöpf–Schulz–Passarge syndrome and how it will continue to affect our environment will also be explored.
| Schöpf–Schulz–Passarge syndrome | |
|---|---|
| Other names | Eyelid cysts, Palmoplantar keratoderma, Hypodontia, and Hypotrichosis |
| Specialty | Medical genetics  |
Schöpf–Schulz–Passarge syndrome is an autosomal recessive condition with punctate symmetric palmoplantar keratoderma, with the keratoderma and fragility of the nails beginning around age 12.: 513 In addition to palmoplantar keratoderma, other symptoms include hypodontia, hypotrichosis, nail dystrophies, and eyelid cysts (apocrine hidrocystomas). Patients may also develop syringofibroadenoma and squamous cell carcinomas.
It has been associated with WNT10A.
See also
- Palmoplantar keratoderma
- List of cutaneous conditions
- List of dental abnormalities associated with cutaneous conditions
- List of cutaneous neoplasms associated with systemic syndromes
References
- ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 778. ISBN 978-1-4160-2999-1.
- ^ Calonje, Eduardo (2012). Mckee's Pathology of the Skin: With Clinical Correlations. Elsevier/Saunders.
- ^ Schöpf E, Schulz HJ, Passarge E (June 1971). "Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait". Birth Defects Orig. Artic. Ser. 7 (8): 219–21. PMID 4281327.
- ^ Bohring A, Stamm T, Spaich C, et al. (July 2009). "WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes". Am. J. Hum. Genet. 85 (1): 97–105. doi:10.1016/j.ajhg.2009.06.001. PMC 2706962. PMID 19559398.
External links
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