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2005 1
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Page 1
Stiff skin syndrome: a clinicopathological study of 31 cases.
Wen X, Chen F, Wang L. Wen X, et al. Eur J Dermatol. 2023 Jun 1;33(3):235-240. doi: 10.1684/ejd.2023.4477. Eur J Dermatol. 2023. PMID: 37594328
BACKGROUND: Stiff skin syndrome (SSS) is a rare disease characterized by sclerosis of the skin. ...
BACKGROUND: Stiff skin syndrome (SSS) is a rare disease characterized by sclerosis of the skin. ...
Sclerodermalike syndromes: Great imitators.
Varjú C, Kumánovics G, Czirják L, Matucci-Cerinic M, Minier T. Varjú C, et al. Clin Dermatol. 2020 Mar-Apr;38(2):235-249. doi: 10.1016/j.clindermatol.2019.10.010. Epub 2019 Oct 24. Clin Dermatol. 2020. PMID: 32513403
Inherited progeria syndromes with early aging (eg, Werner syndrome) and a heterogeneous group of hereditary disorders with either skin thickening (eg, stiff skin syndrome) or atrophy and tightening (eg, acrogeria) can also imitate classic systemic sclerosis ( …
Inherited progeria syndromes with early aging (eg, Werner syndrome) and a heterogeneous group of hereditary disorders with either skin thick …
The stiff skin syndrome: case series, differential diagnosis of the stiff skin phenotype, and review of the literature.
Liu T, McCalmont TH, Frieden IJ, Williams ML, Connolly MK, Gilliam AE. Liu T, et al. Arch Dermatol. 2008 Oct;144(10):1351-9. doi: 10.1001/archderm.144.10.1351. Arch Dermatol. 2008. PMID: 18936399 Review.
BACKGROUND: Stiff skin syndrome is a sclerodermalike disorder that presents in infancy or early childhood with rock-hard skin, limited joint mobility, and mild hypertrichosis in the absence of visceral or muscle involvement, immunologic abnormalities, or vasc …
BACKGROUND: Stiff skin syndrome is a sclerodermalike disorder that presents in infancy or early childhood with rock-har …
Segmental stiff skin syndrome (SSS): Clinical case and a brief review.
Cerejeira D, Bonito F, António AM, Cunha H. Cerejeira D, et al. Australas J Dermatol. 2021 Aug;62(3):380-382. doi: 10.1111/ajd.13589. Epub 2021 Mar 26. Australas J Dermatol. 2021. PMID: 33769553 Review.
Stiff skin syndrome (SSS) is a rare, scleroderma-like condition that is commonly characterised by stony hard skin and limited joint mobility, in the absence of visceral involvement or immunologic abnormalities. ...
Stiff skin syndrome (SSS) is a rare, scleroderma-like condition that is commonly characterised by stony hard skin and l …
Segmental stiff skin syndrome (SSS): A distinct clinical entity.
Myers KL, Mir A, Schaffer JV, Meehan SA, Orlow SJ, Brinster NK. Myers KL, et al. J Am Acad Dermatol. 2016 Jul;75(1):163-8. doi: 10.1016/j.jaad.2016.01.038. Epub 2016 Mar 2. J Am Acad Dermatol. 2016. PMID: 26944597 Review.
BACKGROUND: Stiff skin syndrome (SSS) is a noninflammatory, fibrosing condition of the skin, often affecting the limb girdles. ...
BACKGROUND: Stiff skin syndrome (SSS) is a noninflammatory, fibrosing condition of the skin, often affecting the limb g …
Characteristics and onset of presentation of pediatric stiff skin syndrome: A retrospective cohort study of 11 patients in a tertiary care center.
Sanchez-Espino LF, Sibbald C, Stimec J, Laxer RM, Pope E. Sanchez-Espino LF, et al. Pediatr Dermatol. 2024 Jan-Feb;41(1):16-22. doi: 10.1111/pde.15459. Epub 2023 Oct 20. Pediatr Dermatol. 2024. PMID: 37864376
BACKGROUND/OBJECTIVE: Stiff skin syndrome (SSS) is a rare disorder characterized by "rock hard" indurated skin affecting different body parts. ...
BACKGROUND/OBJECTIVE: Stiff skin syndrome (SSS) is a rare disorder characterized by "rock hard" indurated skin affectin …
New clinical classification of stiff skin syndrome.
Zhao Q, Chu Z, Li L, Feng C, Zhou H, Hu J, Zhao L, Che D, Zhang X, Peng B, Han Y, Geng S. Zhao Q, et al. Arch Dermatol Res. 2024 Jun 6;316(6):333. doi: 10.1007/s00403-024-03090-1. Arch Dermatol Res. 2024. PMID: 38844593
BACKGROUND: Stiff skin syndrome (SSS) is a rare disease characterized by thickened, indurated skin and limited joint movement. ...
BACKGROUND: Stiff skin syndrome (SSS) is a rare disease characterized by thickened, indurated skin and limited joint mo …
A microfibril assembly assay identifies different mechanisms of dominance underlying Marfan syndrome, stiff skin syndrome and acromelic dysplasias.
Jensen SA, Iqbal S, Bulsiewicz A, Handford PA. Jensen SA, et al. Hum Mol Genet. 2015 Aug 1;24(15):4454-63. doi: 10.1093/hmg/ddv181. Epub 2015 May 15. Hum Mol Genet. 2015. PMID: 25979247 Free PMC article.
The majority of mutations affecting the human fibrillin-1 gene, FBN1, result in Marfan syndrome (MFS), a common connective tissue disorder characterised by tall stature, ocular and cardiovascular defects. Recently, stiff skin syndrome (SSS) and a group of syn …
The majority of mutations affecting the human fibrillin-1 gene, FBN1, result in Marfan syndrome (MFS), a common connective tissue disorder c …
Buschke's scleredema and concomitant diseases: report of five cases and literature review.
Lipozencić J, Marasović D, Barisić-Drusko V. Lipozencić J, et al. Acta Dermatovenerol Croat. 2005;13(3):147-52. Acta Dermatovenerol Croat. 2005. PMID: 16146615 Review.
The dermis is thickened because of the increased collagen glycosylation, like that in diabetic stiff skin syndrome. The face is most often involved. In older persons the trunk is usually first involved. ...
The dermis is thickened because of the increased collagen glycosylation, like that in diabetic stiff skin syndrome. The …
Skeletal manifestations of Marfan syndrome associated to heterozygous R2726W FBN1 variant: sibling case report and literature review.
Reyes-Hernández OD, Palacios-Reyes C, Chávez-Ocaña S, Cortés-Malagón EM, Alonso-Themann PG, Ramos-Cano V, Ramírez-Bello J, Sierra-Martínez M. Reyes-Hernández OD, et al. BMC Musculoskelet Disord. 2016 Feb 15;17:79. doi: 10.1186/s12891-016-0935-9. BMC Musculoskelet Disord. 2016. PMID: 26875674 Free PMC article. Review.
FBN1 variants are responsible for the related connective tissue disorders, grouped under the generic term of type-1 fibrillinopathies, which include Marfan syndrome (MFS), MASS syndrome (Mitral valve prolapse, Aortic enlargement, Skin and Skeletal findings, Acromicric dysplasia, …
FBN1 variants are responsible for the related connective tissue disorders, grouped under the generic term of type-1 fibrillinopathies, which …
11 results