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

Year Number of Results
1927 1
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1951 5
1952 3
1953 5
1954 6
1955 5
1956 9
1957 6
1958 7
1959 3
1960 1
1961 5
1962 8
1963 14
1964 12
1965 11
1966 18
1967 16
1968 19
1969 12
1970 15
1971 19
1972 14
1973 16
1974 17
1975 15
1976 19
1977 21
1978 24
1979 21
1980 21
1981 30
1982 25
1983 27
1984 24
1985 28
1986 28
1987 44
1988 32
1989 23
1990 32
1991 24
1992 25
1993 31
1994 40
1995 34
1996 34
1997 36
1998 37
1999 29
2000 47
2001 43
2002 49
2003 49
2004 45
2005 80
2006 84
2007 93
2008 93
2009 90
2010 85
2011 116
2012 161
2013 140
2014 143
2015 192
2016 174
2017 150
2018 179
2019 136
2020 140
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2024 43

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3,443 results

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Page 1
Lenz-Majewski syndrome.
Gorlin RJ, Whitley CB. Gorlin RJ, et al. Radiology. 1983 Oct;149(1):129-31. doi: 10.1148/radiology.149.1.6611917. Radiology. 1983. PMID: 6611917
Lenz-Majewski syndrome is a rare disorder of unknown etiology. The condition is characterized by a disproportionately large head with large fontanels and widely separated sutures that close late. ...
Lenz-Majewski syndrome is a rare disorder of unknown etiology. The condition is characterized by a disproportionately large head with …
Lenz-Majewski syndrome in a patient from Egypt.
Afifi HH, Abdel-Hamid MS, Mehrez MI, El-Kamah G, Abdel-Salam GMH. Afifi HH, et al. Am J Med Genet A. 2019 Oct;179(10):2039-2042. doi: 10.1002/ajmg.a.61327. Epub 2019 Aug 12. Am J Med Genet A. 2019. PMID: 31403251
Lenz-Majewski syndrome (LMS) is an extremely rare type of cutis laxa caused by dominant mutations in PTDSS1 gene. ...
Lenz-Majewski syndrome (LMS) is an extremely rare type of cutis laxa caused by dominant mutations in PTDSS1 gene. ...
Majewski/Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPDII) with generalised microdontia in the 4th millennium BCE Eastern Mediterranean.
Lorentz KO, Branca NM, Lemmers SAM. Lorentz KO, et al. Int J Paleopathol. 2021 Jun;33:158-169. doi: 10.1016/j.ijpp.2021.04.001. Epub 2021 May 3. Int J Paleopathol. 2021. PMID: 33957552
CONCLUSIONS: Differential diagnosis includes pituitary dwarfism and Majewski/Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPDII), which are two types of proportionate dwarfism with presentation of microdontia. This individual appears to display skeletal chan …
CONCLUSIONS: Differential diagnosis includes pituitary dwarfism and Majewski/Microcephalic Osteodysplastic Primordial Dwarfism Type I …
Majewski osteodysplastic primordial dwarfism type II (MOPD II) complicated by stroke: clinical report and review of cerebral vascular anomalies.
Brancati F, Castori M, Mingarelli R, Dallapiccola B. Brancati F, et al. Am J Med Genet A. 2005 Dec 15;139(3):212-5. doi: 10.1002/ajmg.a.31009. Am J Med Genet A. 2005. PMID: 16278902 Review.
Brain neuroimaging disclosed a complex cerebral vascular anomaly (CVA) with stenosis of the right anterior cerebral artery and telangiectatic collateral vessels supplying the cerebral cortex, consistent with moyamoya disease. Based on clinical and skeletal features, a diagnosis o …
Brain neuroimaging disclosed a complex cerebral vascular anomaly (CVA) with stenosis of the right anterior cerebral artery and telangiectati …
[Lenz-Majewski hyperostosis syndrome].
Satokata I. Satokata I. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):205-6. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057197 Review. Japanese. No abstract available.
Lenz-Majewski syndrome and recurrent otitis media: Are they related or not?
Maden Bedel F, Balasar Ö, Erol Aytekin S, Keleş S, Çaksen H. Maden Bedel F, et al. Eur J Med Genet. 2024 Apr;68:104910. doi: 10.1016/j.ejmg.2024.104910. Epub 2024 Jan 21. Eur J Med Genet. 2024. PMID: 38262577 Free article.
Lenz-Majewski hyperostotic dwarfism (LMHD) is a rare condition characterized by intellectual disability, sclerosing bone dysplasia, dysmorphic facial features, brachydactyly, symphalangism and cutis laxa. ...We, hereby, report the case of the first patient with Lenz-Maj …
Lenz-Majewski hyperostotic dwarfism (LMHD) is a rare condition characterized by intellectual disability, sclerosing bone dysplasia, d …
[Short rib-polydactyly syndrome, Majewski type].
Masuno M. Masuno M. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):291-3. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057233 Review. Japanese. No abstract available.
Lenz-Majewski mutations in PTDSS1 affect phosphatidylinositol 4-phosphate metabolism at ER-PM and ER-Golgi junctions.
Sohn M, Ivanova P, Brown HA, Toth DJ, Varnai P, Kim YJ, Balla T. Sohn M, et al. Proc Natl Acad Sci U S A. 2016 Apr 19;113(16):4314-9. doi: 10.1073/pnas.1525719113. Epub 2016 Apr 4. Proc Natl Acad Sci U S A. 2016. PMID: 27044099 Free PMC article.
Lenz-Majewski syndrome (LMS) is a rare disease characterized by complex craniofacial, dental, cutaneous, and limb abnormalities combined with intellectual disability. ...
Lenz-Majewski syndrome (LMS) is a rare disease characterized by complex craniofacial, dental, cutaneous, and limb abnormalities combi …
Lenz-Majewski hyperostotic dwarfism: reexamination of the original patient.
Majewski F. Majewski F. Am J Med Genet. 2000 Aug 14;93(4):335-8. doi: 10.1002/1096-8628(20000814)93:4<335::aid-ajmg14>3.0.co;2-5. Am J Med Genet. 2000. PMID: 10946362
In 1974, Lenz and Majewski gave a short description of a 2-year-old girl with generalized hyperostosis, proximal symphalangism, syndactyly, brachydactyly, cutis laxa, mental retardation, marked hypertelorism, and enamel hypoplasia. This disorder was later named Lenz-Maj …
In 1974, Lenz and Majewski gave a short description of a 2-year-old girl with generalized hyperostosis, proximal symphalangism, synda …
3,443 results