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Year Number of Results
1949 1
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1959 2
1960 1
1961 1
1962 2
1963 3
1964 4
1965 5
1966 1
1967 4
1968 6
1969 10
1970 12
1971 16
1972 14
1973 20
1974 18
1975 26
1976 23
1977 27
1978 24
1979 25
1980 25
1981 26
1982 35
1983 41
1984 35
1985 51
1986 48
1987 37
1988 37
1989 44
1990 64
1991 68
1992 76
1993 85
1994 80
1995 101
1996 129
1997 128
1998 126
1999 120
2000 118
2001 141
2002 119
2003 144
2004 141
2005 148
2006 131
2007 160
2008 158
2009 185
2010 161
2011 216
2012 193
2013 220
2014 216
2015 206
2016 214
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2018 191
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2022 164
2023 150
2024 60

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5,284 results

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Quoted phrase not found in phrase index: "Abnormality of limbs"
Page 1
Campomelic dysplasia.
Jain V, Sen B. Jain V, et al. J Pediatr Orthop B. 2014 Sep;23(5):485-8. doi: 10.1097/BPB.0000000000000058. J Pediatr Orthop B. 2014. PMID: 24800790
Campomelic dysplasia is a rare hereditary congenital osteochondral dysplasia characterized by abnormal bowing of the lower limbs, sex reversal in males, and other skeletal and extraskeletal abnormalities. ...The diagnosis is usually difficult because o …
Campomelic dysplasia is a rare hereditary congenital osteochondral dysplasia characterized by abnormal bowing of the lower …
Persistent sciatic vein.
Büyükertan M, Söztanacı US, Balcıoğlu HA. Büyükertan M, et al. Folia Morphol (Warsz). 2022;81(4):1062-1065. doi: 10.5603/FM.a2021.0091. Epub 2021 Sep 21. Folia Morphol (Warsz). 2022. PMID: 34545558 Free article.
MATERIALS AND METHODS: During the routine dissection of the lower extremities of a Caucasian male cadaver, a case of persistent sciatic vein was found. RESULTS: A persistent sciatic vein originating from the saphenopopliteal junction coursed proximally and laterally …
MATERIALS AND METHODS: During the routine dissection of the lower extremities of a Caucasian male cadaver, a case of persistent sciat …
Craniofrontonasal dysplasia.
Kapusta L, Brunner HG, Hamel BC. Kapusta L, et al. Eur J Pediatr. 1992 Nov;151(11):837-41. doi: 10.1007/BF01957936. Eur J Pediatr. 1992. PMID: 1468459
Seven classical cases had facial features suggestive of frontonasal dysplasia and coronal craniosynostosis. Extracranial abnormalities such as brittle nails with prominent longitudinal grooves or syndactyly of fingers and toes were observed in individual patients. In two f …
Seven classical cases had facial features suggestive of frontonasal dysplasia and coronal craniosynostosis. Extracranial abnormalities …
Brachydactyly.
Temtamy SA, Aglan MS. Temtamy SA, et al. Orphanet J Rare Dis. 2008 Jun 13;3:15. doi: 10.1186/1750-1172-3-15. Orphanet J Rare Dis. 2008. PMID: 18554391 Free PMC article. Review.
Physical therapy and ergotherapy may ameliorate hand function. Prognosis for the brachydactylies is strongly dependent on the nature of the brachydactyly, and may vary from excellent to severely influencing hand function. If brachydactyly forms part of a syndromic entity, …
Physical therapy and ergotherapy may ameliorate hand function. Prognosis for the brachydactylies is strongly dependent on the nature …
Ulnar deficiency.
Miller JK, Wenner SM, Kruger LM. Miller JK, et al. J Hand Surg Am. 1986 Nov;11(6):822-9. doi: 10.1016/s0363-5023(86)80230-1. J Hand Surg Am. 1986. PMID: 3794237
Twenty-nine patients with 34 ulnar deficient limbs were studied; the average follow-up was 7.7 years. To permit early determination of prognosis and decisions regarding treatment, four subtypes of this condition have been identified. ...
Twenty-nine patients with 34 ulnar deficient limbs were studied; the average follow-up was 7.7 years. To permit early determination o …
A multidisciplinary review of triphalangeal thumb.
Potuijt JWP, Galjaard RH, van der Spek PJ, van Nieuwenhoven CA, Ahituv N, Oberg KC, Hovius SER. Potuijt JWP, et al. J Hand Surg Eur Vol. 2019 Jan;44(1):59-68. doi: 10.1177/1753193418803521. Epub 2018 Oct 14. J Hand Surg Eur Vol. 2019. PMID: 30318985 Free PMC article. Review.
Despite being a rare congenital limb anomaly, triphalangeal thumb is a subject of research in various scientific fields, providing new insights in clinical research and evolutionary biology. The findings of triphalangeal thumb can be predictive for other congenit …
Despite being a rare congenital limb anomaly, triphalangeal thumb is a subject of research in various scientific fields, providing ne …
Skewfoot.
Hagmann S, Dreher T, Wenz W. Hagmann S, et al. Foot Ankle Clin. 2009 Sep;14(3):409-34. doi: 10.1016/j.fcl.2009.06.003. Foot Ankle Clin. 2009. PMID: 19712883 Review.
Skewfoot is a rare deformity characterized by forefoot adduction and hindfoot valgus. Its etiology and natural history are unknown, although congenital and syndromic forms are observed. Currently, there is no consent about the treatment of skewfoot. ...
Skewfoot is a rare deformity characterized by forefoot adduction and hindfoot valgus. Its etiology and natural history are unknown, although …
Diagnostic ultrasonography.
McNay MB. McNay MB. Baillieres Clin Obstet Gynaecol. 1987 Mar;1(1):29-53. doi: 10.1016/s0950-3552(87)80022-6. Baillieres Clin Obstet Gynaecol. 1987. PMID: 3311512 Review.
Maternal serum alphafetoprotein screening complements ultrasound in identifying abnormalities, and may also be an indicator of a growth problem in later pregnancy. ...Fetal responses to stimulation can be visualized and quantified. No single parameter may be used alone to …
Maternal serum alphafetoprotein screening complements ultrasound in identifying abnormalities, and may also be an indicator of a grow …
A review of supernumerary and absent limbs and digits of the upper limb.
Klaassen Z, Choi M, Musselman R, Eapen D, Tubbs RS, Loukas M. Klaassen Z, et al. Surg Radiol Anat. 2012 Mar;34(2):101-6. doi: 10.1007/s00276-011-0871-1. Epub 2011 Nov 9. Surg Radiol Anat. 2012. PMID: 22068244 Review.
The development of the upper limbs in a growing embryo is still being elucidated with the recent advent of homeobox genes, but researchers agree that upper limbs develop between stages 12-23 through a complex embryological process. ...Additionally, a number of clini …
The development of the upper limbs in a growing embryo is still being elucidated with the recent advent of homeobox genes, but resear …
Treatment of congenital syndactyly.
Le Hanneur M, Cambon-Binder A, Bachy M, Fitoussi F. Le Hanneur M, et al. Hand Surg Rehabil. 2020 May;39(3):143-153. doi: 10.1016/j.hansur.2019.12.003. Epub 2020 Mar 3. Hand Surg Rehabil. 2020. PMID: 32142954
Defined as the union of two adjacent digits, syndactyly is one of the most common congenital deformities. The severity of the malformation depends on the fusion level, the tissues involved in the union, and whether it is isolated or syndromic. ...When the fingertip is invo …
Defined as the union of two adjacent digits, syndactyly is one of the most common congenital deformities. The severity of the malform …
5,284 results