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Page 1
[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.
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.
Based on clinical and skeletal features, a diagnosis of Majewski osteodysplastic primordial dwarfism type II (MOPD II) was established. Review of 16 published patients with CVA affected by either Seckel syndrome or MOPD II suggested that CVA is preferentially associated to …
Based on clinical and skeletal features, a diagnosis of Majewski osteodysplastic primordial dwarfism type II (MOPD II) was establishe …
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. ...
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 …
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 …
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 …
Non-Majewski short rib-polydactyly syndrome.
Sillence DO. Sillence DO. Am J Med Genet. 1980;7(2):223-9. doi: 10.1002/ajmg.1320070215. Am J Med Genet. 1980. PMID: 7468650
Clinical, radiographic, and morphologic studies of non-Majewski short rib-polydactyly cases show a spectrum of abnormalities. While the findings of Yang et al reported in this journal suggest that a unique change in chondrocytes, namely PAS-positive inclusions, might disti …
Clinical, radiographic, and morphologic studies of non-Majewski short rib-polydactyly cases show a spectrum of abnormalities. While t …
Craniovertebral junction stenosis in Lenz-Majewski syndrome.
Mizuguchi K, Miyazaki O, Nishimura G, Ishigro A. Mizuguchi K, et al. Pediatr Radiol. 2015 Sep;45(10):1567-70. doi: 10.1007/s00247-015-3329-5. Epub 2015 Mar 17. Pediatr Radiol. 2015. PMID: 25779830
We report a girl with Lenz-Majewski syndrome associated with craniovertebral junction stenosis that led to communicating hydrocephalus and cervical myelopathy. ...Close monitoring for craniovertebral junction stenosis is essential to reduce morbidity and mortality in child …
We report a girl with Lenz-Majewski syndrome associated with craniovertebral junction stenosis that led to communicating hydrocephalu …
3,614 results