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

Year Number of Results
1969 2
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1979 3
1982 3
1983 1
1984 3
1986 4
1987 4
1988 1
1990 2
1991 4
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1994 5
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1997 5
1998 6
1999 4
2000 3
2001 7
2002 8
2003 5
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2005 8
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2007 4
2008 8
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2023 14
2024 7

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333 results

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Quoted phrase not found in phrase index: "Polysyndactyly 4"
Page 1
Macrodactyly.
Kotwal PP, Farooque M. Kotwal PP, et al. J Bone Joint Surg Br. 1998 Jul;80(4):651-3. doi: 10.1302/0301-620x.80b4.8489. J Bone Joint Surg Br. 1998. PMID: 9699830
Progressive Postnatal Pansynostosis.
Rogers GF, Greene AK, Proctor MR, Mulliken JB, Goobie SM, Stoler JM. Rogers GF, et al. Cleft Palate Craniofac J. 2015 Nov;52(6):751-7. doi: 10.1597/14-092. Epub 2014 Oct 28. Cleft Palate Craniofac J. 2015. PMID: 25350344
With the exception of one patient with moderate turricephaly, all patients had a relatively normal head shape with cranial indices ranging from 0.72 to 0.93 (mean, 0.81). Patients were diagnosed at an average of 32.4 months; craniosynostosis was suspected based on declinin …
With the exception of one patient with moderate turricephaly, all patients had a relatively normal head shape with cranial indices ranging f …
The Greig cephalopolysyndactyly syndrome.
Biesecker LG. Biesecker LG. Orphanet J Rare Dis. 2008 Apr 24;3:10. doi: 10.1186/1750-1172-3-10. Orphanet J Rare Dis. 2008. PMID: 18435847 Free PMC article. Review.
The primary findings include hypertelorism, macrocephaly with frontal bossing, and polysyndactyly. The polydactyly is most commonly preaxial of the feet and postaxial in the hands, with variable cutaneous syndactyly, but the limb findings vary significantly. ...Ante …
The primary findings include hypertelorism, macrocephaly with frontal bossing, and polysyndactyly. The polydactyly is most commonly p …
Nectinopathies: an emerging group of ectodermal dysplasia syndromes.
Brancati F, Agolini E, Fortugno P. Brancati F, et al. G Ital Dermatol Venereol. 2013 Feb;148(1):59-64. G Ital Dermatol Venereol. 2013. PMID: 23407077 Review.
Cleft Lip/Palate-Ectodermal Dysplasia and Ectodermal Dysplasia-Syndactyly Syndrome are rare congenital disorders caused by recessive mutations in the PVRL1 and PVRL4 genes, respectively. These genes encode nectins 1 and 4, an emerging class of molecules acting in co …
Cleft Lip/Palate-Ectodermal Dysplasia and Ectodermal Dysplasia-Syndactyly Syndrome are rare congenital disorders caused by recessive …
Eye development genes and known syndromes.
Slavotinek AM. Slavotinek AM. Mol Genet Metab. 2011 Dec;104(4):448-56. doi: 10.1016/j.ymgme.2011.09.029. Epub 2011 Sep 29. Mol Genet Metab. 2011. PMID: 22005280 Free PMC article. Review.
This review provides clinical and molecular information for several of the commonest syndromes associated with A/M: Anophthalmia-Esophageal-Genital syndrome, caused by SOX2 mutations, Anophthalmia and pituitary abnormalities caused by OTX2 mutations, Matthew-Wood syndrome caused …
This review provides clinical and molecular information for several of the commonest syndromes associated with A/M: Anophthalmia-Esophageal- …
Hydrocephalus and craniosynostosis.
Cinalli G, Sainte-Rose C, Kollar EM, Zerah M, Brunelle F, Chumas P, Arnaud E, Marchac D, Pierre-Kahn A, Renier D. Cinalli G, et al. J Neurosurg. 1998 Feb;88(2):209-14. doi: 10.3171/jns.1998.88.2.0209. J Neurosurg. 1998. PMID: 9452225
CONCLUSIONS: Abnormal intracranial CSF hydrodynamics was found in 8.1% of the patients (3.4% of whom had received shunts and 4.5% of whom had not). Three types of CSF hydrodynamic disturbance were observed: progressive hydrocephalus with ventricular dilation, nonpro …
CONCLUSIONS: Abnormal intracranial CSF hydrodynamics was found in 8.1% of the patients (3.4% of whom had received shunts and 4 …
Distraction Lengthening of the Apert Thumb.
Upton J, McNamara CT, Ali B, Nuzzi LC, Taghinia AH, Labow BI. Upton J, et al. Plast Reconstr Surg. 2022 Apr 1;149(4):691e-699e. doi: 10.1097/PRS.0000000000008929. Plast Reconstr Surg. 2022. PMID: 35157629
The median follow-up time was 5.0 years, with complications occurring in 36.4 percent (eight out of 22) of patients. A delayed bone union occurred in one patient, and rotational malunion occurred in one patient. CONCLUSION: Although long-term outcomes data are needed, thum …
The median follow-up time was 5.0 years, with complications occurring in 36.4 percent (eight out of 22) of patients. A delayed bone u …
Common Pediatric Congenital Conditions of the Hand.
Kozin SH, Zlotolow DA. Kozin SH, et al. Plast Reconstr Surg. 2015 Aug;136(2):241e-257e. doi: 10.1097/PRS.0000000000001499. Plast Reconstr Surg. 2015. PMID: 26218399 Review.
Accurately diagnose congenital differences that affect the hand. 2. Develop a surgical plan for syndactyly with regard to timing of intervention to prevent progressive deformity and principles to restore the commissure. 3. List the potential complications following polydac …
Accurately diagnose congenital differences that affect the hand. 2. Develop a surgical plan for syndactyly with regard to timing of i …
Single-stage Congenital Polysyndactyly Release: Outcomes and Long-term Followup.
Nazerani S, Nazerani T, Keramati MR. Nazerani S, et al. Tech Hand Up Extrem Surg. 2022 Dec 1;26(4):276-281. doi: 10.1097/BTH.0000000000000399. Tech Hand Up Extrem Surg. 2022. PMID: 35698302
The current surgical strategy for syndactyly is multistage operations in which every other web is released, leaving adjacent webs unoperated for the next stage to avoid a presumed possible digital vascular compromise. ...
The current surgical strategy for syndactyly is multistage operations in which every other web is released, leaving adjacent webs uno …
Familial Poland anomaly revisited.
Baban A, Torre M, Costanzo S, Gimelli S, Bianca S, Divizia MT, Sénès FM, Garavelli L, Rivieri F, Lerone M, Valle M, Ravazzolo R, Calevo MG. Baban A, et al. Am J Med Genet A. 2012 Jan;158A(1):140-9. doi: 10.1002/ajmg.a.34370. Epub 2011 Nov 22. Am J Med Genet A. 2012. PMID: 22110015 Review.
Group1: true familial PA (F-PA): pectoral muscle defects with familial recurrence: 8(4.2%). Group2: familial Poland-like anomaly families (F-PLA): PA index case and 1 relative(s) showing normal pectoral muscles but ULA and/or TA common in PA: 16(8.4%). Group3: spora …
Group1: true familial PA (F-PA): pectoral muscle defects with familial recurrence: 8(4.2%). Group2: familial Poland-like anomaly fami …
333 results