๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Lethal osteosclerotic skeletal dysplasia with intracellular inclusion bodies

โœ Scribed by Brodie, Steven G.; Lachman, Ralph S.; McGovern, Margaret M.; Mekikian, Pertchoui B.; Wilcox, William R.


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
65 KB
Volume
83
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19990423)83:5<372::aid-ajmg6>3.0.co;2-j

No coin nor oath required. For personal study only.

โœฆ Synopsis


We report an apparently previously undescribed form of lethal osteosclerotic skeletal dysplasia in a 30-week male fetus with micromelic shortness of the limbs. Radiographic findings at necropsy included increased density in all bones, most marked in the skull, mandible, and pubis. The ribs were very short, abnormally modeled, and wide anteriorly. The vertebrae were posteriorly hypoplastic and wedged, particularly in the cervical and lumbar regions. The femora and tibiae were short with wide distal metaphyses, undermodeled diaphyses, and coxa vara. The humeri, radii, and ulnae were also short and undermodeled with proximal and distal flare. Chondro-osseous morphology showed short chondrocyte columns, extension of hypertrophic cells into the metaphysis, and overgrowth of perichondral bone. In the resting cartilage there were large chondrocytes containing a homogeneous material staining pink with von Kossa trichrome, gray with toluidine blue, and black with silver methenamine. The cortical bone was lacking and the trabecular bone was hypercellular, thick, and coarse. Ultrastructurally, the resting zone chondrocytes were large and round with condensed chromatin and dilated loops of rough endoplasmic reticulum. The radiographic and histopathologic findings in this case are unique and differ from those seen in other reported lethal osteosclerotic skel-etal dysplasias. Am. J. Med. Genet. 83:372-377, 1999.


๐Ÿ“œ SIMILAR VOLUMES


Lethal osteosclerotic osteochondrodyspla
โœ Brodie, Steven G.; Lachman, Ralph S.; Jewell, Ann F.; Winkler, Carey L.; Nolasco ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 40 KB ๐Ÿ‘ 1 views

We report on a previously undescribed form of lethal osteosclerotic skeletal dysplasia in sibs from nonconsanguineous parents. Radiographic findings included increased density in the base of the skull, clavicles, vertebrae, ribs, and the metaphyseal regions of the long bones. There was midface hypop

Antenatal diagnosis of lethal skeletal d
โœ Tretter, Anne E.; Saunders, Roger C.; Meyers, Carol M.; Dungan, Jeffrey S.; Grum ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 30 KB ๐Ÿ‘ 2 views

Lethal skeletal dysplasias (LSD) are a heterogeneous group of rare but important genetic disorders characterized by abnormal growth and development of bone and cartilage. We describe the diagnosis and outcome of 29 cases of lethal skeletal dysplasias evaluated between January 1989 and December 1996

cover
โœ Dobi Cross ๐Ÿ“‚ Fiction ๐Ÿ“… 2018 ๐Ÿ› Luxhaven Publishing ๐ŸŒ English โš– 80 KB
cover
โœ Cross, Dobi ๐Ÿ“‚ Fiction ๐Ÿ“… 2018 ๐Ÿ› Luxhaven Publishing ๐ŸŒ English โš– 80 KB
Lethal syndrome of skeletal dysplasia an
โœ Khosravi, Mahvash; Weaver, David D.; Bull, Marilyn J.; Lachman, Ralph; Rimoin, D ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 56 KB ๐Ÿ‘ 2 views

We describe 3 sibs (2 males and 1 female) with multiple congenital anomalies, poor growth, seizures, and progressive central nervous system (CNS) degeneration leading to death in infancy. Radiographic changes in all 3 were similar, and included moderate shortness of long bones, platyspondyly, and hy

Platyspondylic lethal skeletal dysplasia
โœ Brodie, Steven G.; Kitoh, Hiroshi; Lachman, Ralph S.; Nolasco, Loyda M.; Mekikia ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 26 KB

The platyspondylic lethal skeletal dysplasias (PLSDs) are a heterogeneous group of short-limb dwarfing conditions. The most common form of PLSD is thanatophoric dysplasia (TD), which has been divided into two types (TD1 and TD2). Three other types of PLSD, or TD variants (San Diego, Torrance, and Lu