Radiological signs of Leri-Weill dyschondrosteosis in Turner syndrome

Hormone Research

Volumn 55, Issue 2, 2001, Pages 71-76

  Binder, Gerhard ^a   Fritsch, Heidi ^a   Schweizer, Roland ^a   Ranke, Michael B ^a  

^a UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

Author keywords

Dyschondrosteosis; Leri Weill syndrome; Madelung deformity; Turner syndrome

Indexed keywords

ESTROGEN; GROWTH HORMONE; HUMAN GROWTH HORMONE; OXANDROLONE;

ADOLESCENT; ADULT; ARTICLE; BONE MALFORMATION; CARPAL BONE; DISEASE ASSOCIATION; DYSCHONDROSTEOSIS; EPIPHYSIS; ESTROGEN THERAPY; FEMALE; HORMONAL THERAPY; HORMONE DEFICIENCY; HUMAN; LEFT HANDEDNESS; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; RADIOGRAPHY; RADIUS; TURNER SYNDROME;

ADOLESCENT; ADULT; CARPAL BONES; CHILD; FEMALE; GROWTH DISORDERS; HAND; HOMEODOMAIN PROTEINS; HUMAN GROWTH HORMONE; HUMANS; METACARPUS; OSTEOCHONDRODYSPLASIAS; RETROSPECTIVE STUDIES; SYNDROME; TURNER SYNDROME; X CHROMOSOME;

EID: 0034891877     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000049973     Document Type: Article

References (18)

1. SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
2. Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis
3. Une affection congénitale et symétrique du développement osseux: La dyschondrostéose
4. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
5. PHOG, a candidate gene for involvement in the short stature of Turner syndrome
6. Turner Syndrome
7. Skeletal features and growth pattern in 14 patients with haploinsufficiency of SHOX: Implications for the development of Turner syndrome
8. Phenotypic variation and genetic heterogeneity in Leri- Weill syndrome
9. Identification of short stature caused by SHOX defects and therapeutic effect of recombinant human growth hormone
10. The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
11. Diagnostic value of hand x-rays in Turner's syndrome
12. Dyschondrosteosis. A hereditable bone dysplasia with characteristic roentgenographic features
13. The roentgen appearance of the hand and wrist in gonadal dysgenesis
14. Madelung deformity in skeletally immature patients: Morphologic assessment using radiography, CT, and MRI
15. Pediatric endocrinology update: An overview. The essential roles of estrogens in pubertal growth, epiphyseal fusion and bone turnover: Lessons from mutations in the genes for aromatase and the estrogen receptor
16. Prediction of growth response in children with various growth disorders treated with growth hormone: Analyses of data from the Kabi Pharmacia International Growth Study