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Autopsy case of microcephalic osteodysplastic primordial ?dwarfism? type II

✍ Scribed by Fukuzawa, Ryuji ;Sato, Seiji ;Sullivan, Michael J. ;Nishimura, Gen ;Hasegawa, Tomonobu ;Matsuo, Nobutake

Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
177 KB
Volume
113
Category
Article
ISSN
0148-7299

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πŸ“œ SIMILAR VOLUMES

Microcephalic osteodysplastic primordial
Microcephalic osteodysplastic primordial dwarfism type ii: Report of three cases and review
✍ Majewski, Frank; Goecke, Timm O. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 51 KB πŸ‘ 1 views

We report on three further patients with microcephalic osteodysplastic dwarfism type II. All children have marked intrauterine and postnatal growth failure, microcephaly, and mental and statomotor retardation. They are disproportionately short statured due to short limbs. Characteristic skeletal abn

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✍ Sigaudy, S.; Toutain, A.; Moncla, A.; Fredouille, C.; BourliοΏ½re, B.; Ayme, S.; P πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 86 KB πŸ‘ 1 views

Microcephalic and osteodysplastic primordial dwarfism (MODP) types I, II, and III were defined by Majewski et al. in 1982. This group of syndromes was characterized by intrauterine growth retardation, microcephaly, and typical facial appearance with prominent nose and micrognathia. Type II was clear