Literature DB >> 6464678

Neuropathologic findings in thanatophoric dysplasia.

K L Ho, C H Chang, S S Yang, J L Chason.   

Abstract

Neuropathologic study of eight cases of thanatophoric dysplasia (dwarfism) reveals developmental abnormalities including hypoplasia of posterior fossa, megalencephaly, cerebral gyral disorganization, hippocampal malformation, neuronal heterotopia, nuclear dysplasia, and abnormal axonal bundles. There are no noticeable differences in CNS abnormalities between thanatophoric dysplasia with and without cloverleaf skull (Kleeblattschädel). The CNS abnormalities, likely the result of abnormal neuronal migration and cytoarchitectonic disarrangement, are apparently not caused by skeletal abnormalities. The observation suggests that CNS abnormalities represent a characteristic and distinct manifestation of thanatophoric dysplasia.

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Year:  1984        PMID: 6464678     DOI: 10.1007/bf00685248

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  44 in total

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Journal:  Lancet       Date:  1974-08-31       Impact factor: 79.321

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Authors:  V S Caviness; P Evrard; G Lyon
Journal:  Acta Neuropathol       Date:  1978-01-19       Impact factor: 17.088

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Authors:  R L Sidman; P Rakic
Journal:  Brain Res       Date:  1973-11-09       Impact factor: 3.252

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Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

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Authors:  D O Sillence; W A Horton; D L Rimoin
Journal:  Am J Pathol       Date:  1979-09       Impact factor: 4.307

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  7 in total

1.  Thanatophoric dysplasia in identical twins.

Authors:  A S Knisely
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

2.  Cerebral abnormalities in thanatophoric dysplasia.

Authors:  C L Coulter; R W Leech; R A Brumback; G B Schaefer
Journal:  Childs Nerv Syst       Date:  1991-02       Impact factor: 1.475

3.  Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype.

Authors:  G A Bellus; E B Spector; P W Speiser; C A Weaver; A T Garber; C R Bryke; J Israel; S S Rosengren; M K Webster; D J Donoghue; C A Francomano
Journal:  Am J Hum Genet       Date:  2000-10-27       Impact factor: 11.025

4.  A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene.

Authors:  P L Tavormina; G A Bellus; M K Webster; M J Bamshad; A E Fraley; I McIntosh; J Szabo; W Jiang; E W Jabs; W R Wilcox; J J Wasmuth; D J Donoghue; L M Thompson; C A Francomano
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

5.  Prospective assessment of risks for cervicomedullary-junction compression in infants with achondroplasia.

Authors:  R M Pauli; V K Horton; L P Glinski; C A Reiser
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

6.  Thanatophoric dysplasia: case report of an autopsy complemented by postmortem computed tomographic study.

Authors:  Éber Emanuel Mayoral; Regina Schultz; Sérgio Rosemberg; Lisa Suzuki; Luiz Antonio Nunes de Oliveira; Fernando Uliana Kay
Journal:  Autops Case Rep       Date:  2014-06-30

7.  Enhanced FGFR3 activity in postmitotic principal neurons during brain development results in cortical dysplasia and axonal tract abnormality.

Authors:  Jui-Yen Huang; Bruna Baumgarten Krebs; Marisha Lynn Miskus; May Lin Russell; Eamonn Patrick Duffy; Jason Michael Graf; Hui-Chen Lu
Journal:  Sci Rep       Date:  2020-10-28       Impact factor: 4.379

  7 in total

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