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
1990 1
1992 1
1993 2
1995 1
1997 1
2000 1
2001 1
2003 1
2004 1
2007 1
2008 1
2012 1
2013 2
2014 1
2015 1
2016 1
2017 1
2018 2
2019 4
2020 3
2021 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

24 results

Results by year

Filters applied: . Clear all
Page 1
Forefoot malformations, deformities and other congenital defects in children.
Rampal V, Giuliano F. Rampal V, et al. Orthop Traumatol Surg Res. 2020 Feb;106(1S):S115-S123. doi: 10.1016/j.otsr.2019.03.021. Epub 2019 Oct 21. Orthop Traumatol Surg Res. 2020. PMID: 31648997 Free article. Review.
These deformities are more easily cured when they occur later during the fetal period. When the anomaly is bilateral, a genetic origin must be considered. There are two main entities under the term "deformity": metatarsus adductus and skewfoot (aka "Z"-foot or serpentine f …
These deformities are more easily cured when they occur later during the fetal period. When the anomaly is bilateral, a genetic origi …
Tarsal coalition.
Bohne WH. Bohne WH. Curr Opin Pediatr. 2001 Feb;13(1):29-35. doi: 10.1097/00008480-200102000-00005. Curr Opin Pediatr. 2001. PMID: 11176240 Review.
Although most coalitions are congenital, as the consequence of autosomal dominant inheritance, coalitions also can be acquired by degenerative joint disease, inflammatory arthritis, infection, and clubfoot deformities. Fifty percent of all coalitions are bilateral. …
Although most coalitions are congenital, as the consequence of autosomal dominant inheritance, coalitions also can be acquired by degenerati …
Congenital idiopathic clubfoot deformities.
Kyzer SP, Stark SL. Kyzer SP, et al. AORN J. 1995 Mar;61(3):492-506; quiz 508-12. doi: 10.1016/s0001-2092(06)63739-3. AORN J. 1995. PMID: 7778903 Review.
In congenital idiopathic clubfoot (ie, talipes equinovarus), the infant's foot points downward (ie, equinus) and turns inward (ie, varus), while the forefoot curls toward the heel (ie, adduction). This congenital disorder has an incidence of 1 in 400 live bir …
In congenital idiopathic clubfoot (ie, talipes equinovarus), the infant's foot points downward (ie, equinus) and turns …
[Congenital multiple arthrogryposis].
Parsch K, Pietrzak S. Parsch K, et al. Orthopade. 2007 Mar;36(3):281-90; quiz 291. doi: 10.1007/s00132-007-1044-0. Orthopade. 2007. PMID: 17323063 Review. German.
The club foot and the rocker-bottom foot need sophisticated conservative and operative treatments. If conservative manipulation of bilateral extension contractures of the elbow fails operative treatment is carried out on the dominant side. ...
The club foot and the rocker-bottom foot need sophisticated conservative and operative treatments. If conservative manipulation of bilate
Osteogenesis imperfecta and clubfoot-a rare combination: Case report and review of the literature.
Persiani P, Ranaldi FM, Martini L, Zambrano A, Celli M, D'Eufemia P, Villani C. Persiani P, et al. Medicine (Baltimore). 2016 Aug;95(31):e4505. doi: 10.1097/MD.0000000000004505. Medicine (Baltimore). 2016. PMID: 27495102 Free PMC article. Review.
This paper presents the case of a child with OI type IV who, at birth, was also diagnosed with a severe clubfoot (congenital talipes equinovarus) grade III. Patient's mother also suffers from OI type IV. ...When the patient was 3 months of age, we decided to …
This paper presents the case of a child with OI type IV who, at birth, was also diagnosed with a severe clubfoot (congenital talip
Management of hip contractures and dislocations in arthrogryposis.
Stilli S, Antonioli D, Lampasi M, Donzelli O. Stilli S, et al. Musculoskelet Surg. 2012 Jun;96(1):17-21. doi: 10.1007/s12306-012-0180-9. Epub 2012 Jan 26. Musculoskelet Surg. 2012. PMID: 22278604 Review.
For unilateral dislocations, open reduction is indicated to provide a level pelvis, even though the risk of stiffness, avascular necrosis and redislocation is significant. Indications for surgical reduction of bilateral dislocations are more controversial: an adequate eval …
For unilateral dislocations, open reduction is indicated to provide a level pelvis, even though the risk of stiffness, avascular necrosis an …
A TRPV4 mutation caused Charcot-Marie-Tooth disease type 2C with scapuloperoneal muscular atrophy overlap syndrome and scapuloperoneal spinal muscular atrophy in one family: a case report and literature review.
Chen H, Sun C, Zheng Y, Yin J, Gao M, Zhao C, Lin J. Chen H, et al. BMC Neurol. 2023 Jun 30;23(1):250. doi: 10.1186/s12883-023-03260-0. BMC Neurol. 2023. PMID: 37391745 Free PMC article. Review.
Nerve conduction study showed axon damage in both motor and sensory nerves. Sensory nerve action potentials could not be evoked in bilateral sural or superficial peroneal nerves. He was diagnosed with Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy …
Nerve conduction study showed axon damage in both motor and sensory nerves. Sensory nerve action potentials could not be evoked in bilate
DSE associated musculocontractural EDS, a milder phenotype or phenotypic variability.
Schirwani S, Metcalfe K, Wagner B, Berry I, Sobey G, Jewell R. Schirwani S, et al. Eur J Med Genet. 2020 Apr;63(4):103798. doi: 10.1016/j.ejmg.2019.103798. Epub 2019 Oct 23. Eur J Med Genet. 2020. PMID: 31655143 Review.
Analysing clinical exome data, a homozygous pathogenic DSE variant, c.1150_1157del p.(Pro384Trpfs*9), was identified in a 32 year old man with bilateral congenital talipes equinovarus, characteristic facial features, myopia, hyperextensible skin at the elbows …
Analysing clinical exome data, a homozygous pathogenic DSE variant, c.1150_1157del p.(Pro384Trpfs*9), was identified in a 32 year old man wi …
Congenital cavitary optic disc anomaly and Axenfeld's anomaly in Wolf-Hirschhorn syndrome: A case report and review of the literature.
Ali MH, Azar NF, Aakalu V, Chau FY, Abbasian J, Setabutr P, Maumenee IH. Ali MH, et al. Ophthalmic Genet. 2018 Apr;39(2):271-274. doi: 10.1080/13816810.2017.1408850. Epub 2017 Dec 4. Ophthalmic Genet. 2018. PMID: 29199884 Free PMC article. Review.
Systemic findings included "Greek warrior helmet" facies, hypotonia, cleft palate, neonatal tooth eruption, talipes equinovarus, bilateral clinodactyly, clitoromegaly, partial agenesis of the corpus callosum, bilateral renal hypoplasia, and two atrial …
Systemic findings included "Greek warrior helmet" facies, hypotonia, cleft palate, neonatal tooth eruption, talipes equinovarus
Chromosome 18q-syndrome and 1p terminal duplication in a patient with bilateral vesico-ureteral reflux: case report and literature revision.
Brandigi E, Molinaro F, Bulotta AL, Angotti R, Pavone M, Messina M. Brandigi E, et al. Ital J Pediatr. 2013 Jan 23;39:6. doi: 10.1186/1824-7288-39-6. Ital J Pediatr. 2013. PMID: 23343423 Free PMC article. Review.
VUR may occur isolated or in association with other congenital abnormalities or as part of syndromic entities. We present a patient with a bilateral primary VUR, syndromic disease caused by a large deletion of 18q (18q21.3-qter) and terminal duplication of 1p (1p36.32-p36. …
VUR may occur isolated or in association with other congenital abnormalities or as part of syndromic entities. We present a patient with a …
24 results