
Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma.
Publication
, Journal Article
Fryburg, JS; Sidhu-Malik, N
Published in: J Am Acad Dermatol
November 1995
Mandibuloacral dysplasia is a rare syndrome characterized by mandibular hypoplasia, delayed cranial suture closure, dysplastic clavicles, abbreviated, club-shaped terminal phalanges, acroosteolysis, atrophy of the skin over the hands and feet, and poikilodermatous skin changes. We describe the cases of two siblings with features of mandibuloacral dysplasia who as children were considered to have hereditary sclerosing poikiloderma. On their reevaluation as adults, the clinical features of their condition were perceived to be compatible with mandibuloacral dysplasia.
Duke Scholars
Published In
J Am Acad Dermatol
DOI
ISSN
0190-9622
Publication Date
November 1995
Volume
33
Issue
5 Pt 2
Start / End Page
900 / 902
Location
United States
Related Subject Headings
- Syndrome
- Rothmund-Thomson Syndrome
- Pigmentation Disorders
- Osteoarthropathy, Secondary Hypertrophic
- Nuclear Family
- Mandible
- Male
- Humans
- Follow-Up Studies
- Fingers
Citation
APA
Chicago
ICMJE
MLA
NLM
Fryburg, J. S., & Sidhu-Malik, N. (1995). Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma. J Am Acad Dermatol, 33(5 Pt 2), 900–902. https://doi.org/10.1016/0190-9622(95)90432-8
Fryburg, J. S., and N. Sidhu-Malik. “Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma.” J Am Acad Dermatol 33, no. 5 Pt 2 (November 1995): 900–902. https://doi.org/10.1016/0190-9622(95)90432-8.
Fryburg JS, Sidhu-Malik N. Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma. J Am Acad Dermatol. 1995 Nov;33(5 Pt 2):900–2.
Fryburg, J. S., and N. Sidhu-Malik. “Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma.” J Am Acad Dermatol, vol. 33, no. 5 Pt 2, Nov. 1995, pp. 900–02. Pubmed, doi:10.1016/0190-9622(95)90432-8.
Fryburg JS, Sidhu-Malik N. Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma. J Am Acad Dermatol. 1995 Nov;33(5 Pt 2):900–902.

Published In
J Am Acad Dermatol
DOI
ISSN
0190-9622
Publication Date
November 1995
Volume
33
Issue
5 Pt 2
Start / End Page
900 / 902
Location
United States
Related Subject Headings
- Syndrome
- Rothmund-Thomson Syndrome
- Pigmentation Disorders
- Osteoarthropathy, Secondary Hypertrophic
- Nuclear Family
- Mandible
- Male
- Humans
- Follow-Up Studies
- Fingers