| Albright's hereditary osteodystrophy. | |
| | |
MedLine Citation:
|
PMID: 6246707 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
The authors observed different clinical forms of Albright's hereditary osteodystrophy in 4 members of a family (two sisters, their mother and the maternal grandfather). The sisters were affected by pseudohypoparathyroidism type I, the older manifested the hypocalcemic variety, the younger the normocalcemic variety; the mother and the grandfather presented only with short stature and subcutaneous calcifications. The variety of clinical and biochemical alterations observed in these 3 generations supports evidence that Albright's hereditary osteodystrophy has a broad spectrum and that distinctions between the various forms of pseudohypoparathyroidsim should not be rigidly considered. |
| | |
Authors:
|
B Boscherini; G Coen; G Bianchini; G Gallucci; P Ballanti; A M Pasquino; F Piccolo; M L Manca Bitti; G L Spadoni |
Related Documents
:
|
16396427 - Prenatal determinants of schizophrenia: what we have learned thus far? 16531737 - Distinctive collection of fetal anomalies: cleft lip and palate, multicystic dysplastic... 8494487 - Homosexual orientation in twins: a report on 61 pairs and three triplet sets. 16171467 - Is there increased monozygotic twinning after assisted reproductive technology? 6831537 - Development of the capillary system in the neurohypophysis of the rat. 14764967 - Fetal hemolytic disease due to anti-rh17 alloimmunization. |
Publication Detail:
|
Type: Journal Article |
Journal Detail:
|
Title: Acta paediatrica Scandinavica Volume: 69 ISSN: 0001-656X ISO Abbreviation: Acta Paediatr Scand Publication Date: 1980 May |
Date Detail:
|
Created Date: 1980-07-28 Completed Date: 1980-07-28 Revised Date: 2009-11-11 |
Medline Journal Info:
|
Nlm Unique ID: 0000211 Medline TA: Acta Paediatr Scand Country: SWEDEN |
Other Details:
|
Languages: eng Pagination: 305-9 Citation Subset: IM |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Adult Aged Body Height Calcium / blood Carpal Bones / radiography Child Cyclic AMP / blood Female Fibrous Dysplasia of Bone / genetics* Fibrous Dysplasia, Polyostotic / genetics* Humans Infant Male Middle Aged Parathyroid Hormone / blood Phosphorus / blood Pseudohypoparathyroidism / genetics |
| Chemical | |
Reg. No./Substance:
|
0/Parathyroid Hormone; 60-92-4/Cyclic AMP; 7440-70-2/Calcium; 7723-14-0/Phosphorus |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Differentiated care of hip fracture in the elderly. Mean hospital days and results of rehabilitation...
Next Document: Enhanced renal tubular calcium reabsorption independent of parathormone activity, in children on lon...