Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
2000 1
2001 1
2003 1
2007 1
2013 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

6 results

Results by year

Filters applied: . Clear all
Page 1
Unpredictability of hip behavior in Dyggve-Melchior-Clausen syndrome: a mid-term assessment of siblings.
Nectoux E, Hocquet B, Fron D, Mezel A, Paris A, Herbaux B. Nectoux E, et al. Orthop Traumatol Surg Res. 2013 Oct;99(6):745-8. doi: 10.1016/j.otsr.2013.04.006. Epub 2013 Sep 12. Orthop Traumatol Surg Res. 2013. PMID: 24035654 Free article. Review.
Dyggve-Melchior-Clausen syndrome is a rare spondylo-epiphyseal disease, which almost constantly leads to both bilateral hip degeneration and dislocation. ...
Dyggve-Melchior-Clausen syndrome is a rare spondylo-epiphyseal disease, which almost constantly leads to both bi …
[Dyggve-Melchior-Clausen syndrome].
Okamoto N. Okamoto N. Ryoikibetsu Shokogun Shirizu. 2001;(33):586-7. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462582 Review. Japanese. No abstract available.
[Dyggve-Melchior-Clausen syndrome].
Kondoh T, Matsumoto T. Kondoh T, et al. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):175-6. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057185 Review. Japanese. No abstract available.
[Dyggve-Melchior-Clausen syndrome: presentation of a case with a mutation of possible Spanish origin].
Martínez-Frías ML, Cormier-Daire V, Cohn DH, Mendioroz J, Bermejo E, Mansilla E. Martínez-Frías ML, et al. Med Clin (Barc). 2007 Feb 3;128(4):137-40. doi: 10.1157/13098019. Med Clin (Barc). 2007. PMID: 17288936 Review. Spanish.
BACKGROUND AND OBJECTIVE: The Dyggve-Melchior-Clausen syndrome is a progressive spondyloepimetaphyseal dysplasia characterized by a short trunk dwarfism, barrel chest, sternal protrusion, kyphoscoliosis, severe platyspondyly, with a central constrictio …
BACKGROUND AND OBJECTIVE: The Dyggve-Melchior-Clausen syndrome is a progressive spondyloepimetaphyseal dysplasia …
[Dyggve-Melchior-Clausen syndrome. Case report and review of the literature].
Schlaepfer R, Rampini S, Wiesmann U. Schlaepfer R, et al. Helv Paediatr Acta. 1981;36(6):543-59. Helv Paediatr Acta. 1981. PMID: 7037691 Review. German.
The Dyggve-Melchior-Clausen syndrome is inherited in an autosomal recessive mode and is clinically characterized by mental retardation, small stature mainly due to a short vertebral column with thoracal kyphosis, protruding sternum, reduced articular m …
The Dyggve-Melchior-Clausen syndrome is inherited in an autosomal recessive mode and is clinically characterized …