Leg Length Discrepancy in Patients With Lower Extremity Cutis Marmorata Telangiectatica Congenita: A Multicenter Retrospective Study
- PMID: 41705466
- DOI: 10.1111/pde.70159
Leg Length Discrepancy in Patients With Lower Extremity Cutis Marmorata Telangiectatica Congenita: A Multicenter Retrospective Study
Abstract
Objectives: To assess the frequency of leg length discrepancy (LLD) in patients with lower extremity cutis marmorata telangiectatica congenita (CMTC), describe associated findings, and characterize LLD management.
Methods: We conducted a retrospective chart review of patients diagnosed with lower extremity CMTC by dermatology and evaluated by orthopedics at Boston Children's Hospital and Children's Hospital of Philadelphia from 1997 to 2024. LLD was assessed by orthopedic examination and/or radiographic imaging. Major LLD was defined as ≥ 2 cm at any age, or between 1 and 2 cm in children 4 years old or younger. Mild LLD was defined as < 2 cm, except when ≥ 1 cm was present by age 4. Kaplan-Meier analysis estimated the probability of developing major LLD by age 15.
Results: Twenty-eight patients with lower extremity CMTC were included. LLD was identified in 12 of 28 patients (43%), including 8 confirmed radiographically and 4 diagnosed by clinical assessment alone. Two (7%) were classified as major and 10 (36%) as mild. Limb hypoplasia occurred in 18 of 28 patients (64%). Kaplan-Meier analysis estimated a 7.1% cumulative risk of major LLD by age 15. Three of 12 patients (25%) with LLD were prescribed shoe lifts.
Conclusion: LLD is common among patients with lower extremity CMTC. Early orthopedic assessment may facilitate timely intervention.
Keywords: CMTC; cutis marmorata telangiectatica congenita; leg length discrepancy; limb hypoplasia.
© 2026 Wiley Periodicals LLC.
References
-
- D. D. Picascia and N. B. Esterly, “Cutis Marmorata Telangiectatica Congenita: Report of 22 Cases,” Journal of the American Academy of Dermatology 20, no. 6 (1989): 1098–1104.
-
- R. Levy and J. M. Lam, “Cutis Marmorata Telangiectatica Congenita: A Mimicker of a Common Disorder,” Canadian Medical Association Journal 183, no. 4 (2011): E249–E251.
-
- M. K. Spraker, C. Stack, and N. B. Esterly, “Congenital Generalized Fibromatosis: A Review of the Literature and Report of a Case Associated With Porencephaly, Hemiatrophy, and Cutis Marmorata Telangiectatica Congenita,” Journal of the American Academy of Dermatology 10, no. 2 Pt 2 (1984): 365–371.
-
- C. Downey, D. Metry, M. C. Garzon, L. K. Morales, and E. Baselga, “Cutis Marmorata Telangiectatica Congenita: Incidence of Extracutaneous Manifestations and a Proposed Clinical Definition,” Pediatric Dermatology 40, no. 5 (2023): 820–828.
-
- A. K. Kienast and P. H. Hoeger, “Cutis Marmorata Telangiectatica Congenita: A Prospective Study of 27 Cases and Review of the Literature With Proposal of Diagnostic Criteria,” Clinical and Experimental Dermatology 34, no. 3 (2009): 319–323.
LinkOut - more resources
Full Text Sources
