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D. Martin, J. Bourdillon. Un cas de tétanie idiopathique chronique. Échec thérapeutique de la graffe d'un adénome parathyroïdien. Revue médicale de la Suisse romande, Lausanne, 1940, 60: 1166-1177.
693:
F. Albright, C. H. Burnett, P. H. Smith, et al. Pseudo-hypoparathyroidism-example of 'Seabright-Bantam syndrome'; report of three cases. Endocrinology, Baltimore, 1942, 30: 922-932.
477:
Garavelli L; Pedori S; Zanacca C; et al. (April 2005). "Albright's hereditary osteodystrophy (pseudohypoparathyroidism type Ia): clinical case with a novel mutation of GNAS1".
285:
Treatment consists of maintaining normal levels of calcium, phosphorus, and vitamin D. Phosphate binders, supplementary calcium and vitamin D will be used as required.
359:
301:
chicken, which demonstrates an analogous hormone insensitivity. Much less commonly, the term Martin-Albright syndrome is used, this refers to Eric Martin.
19:
This article is about the subtype of pseudohypoparathyroidism known as
Albright's hereditary osteodystrophy. For the genetically-related condition, see
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The mechanism of this condition is due to Gs signaling decrease in hormones having to do with
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The diagnosis of
Albright's hereditary osteodystrophy is based on the following exams below:
744:
Henderson, Katherine E.; Baranski, Thomas J.; Bickel, Perry E.; Clutter, William E. (2009).
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362:. Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. Archived from
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which is when a signal from outside cell causes change within the cell (in function).
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Knowledge articles incorporating text from the 20th edition of Gray's
Anatomy (1918)
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Thakker, Rajesh V.; Whyte, Michael P.; Eisman, John; Igarashi, Takashi (2013).
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Albright's hereditary osteodystrophy has an autosomal dominant pattern of
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647:"Urinary 3'5' cyclic AMP. Diagnostic test in pseudohypoparathyroidism"
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type 1A; this is a condition in which the body does not respond to
47:
505:"OMIM Entry - # 103580 - PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A"
97:
calcium, phosphorus, PTH, Urine test for phosphorus and cyclic AMP
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Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007).
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591:"Pseudohypoparathyroidism: MedlinePlus Medical Encyclopedia"
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Individuals with
Albright hereditary osteodystrophy exhibit
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150:
747:
The
Washington Manual Endocrinology Subspecialty Consult
776:
644:
645:Tze, W. J.; Saunders, J.; Drummond, G. I. (1975).
431:. Philadelphia, PA: Elsevier. pp. chap 572.
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196:, characteristically shortened fourth and fifth
158:The disorder is characterized by the following:
536:"Pathways of Intracellular Signal Transduction"
16:Form of osteodystrophy and a rare human disease
897:
719:Genetics of Bone Biology and Skeletal Disease
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223:pattern, and seems to be associated with a
911:
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204:, and often mild intellectual deficiency.
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37:
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105:Phosphate binders, supplementary calcium
79:Choroid plexus calcification, Full cheeks
873:Albright's hereditary osteodystrophy
426:
149:
1137:Hypertrophic pulmonary osteoarthropathy
445:
387:
1451:
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429:Nelson Textbook of Pediatrics. 20th ed
360:"Albright's hereditary osteodystrophy"
327:This article incorporates text in the
216:. It is thought to be inherited in an
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750:. Lippincott Williams & Wilkins.
601:from the original on 13 February 2017
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422:
420:
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515:from the original on 18 January 2017
383:
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124:Albright's hereditary osteodystrophy
32:Albright's hereditary osteodystrophy
583:
13:
709:
417:
347:
212:This condition is associated with
14:
1490:
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456:. St. Louis: Mosby. p. 657.
390:"Alpha hereditary Osteodystrophy"
378:
1479:Diseases named after discoverers
855:
321:
1198:Infantile cortical hyperostosis
696:
687:
638:
627:from the original on 2017-02-13
613:
572:from the original on 2020-05-16
542:from the original on 2018-04-05
406:from the original on 2021-04-26
293:The disorder bears the name of
1132:Complex regional pain syndrome
553:
527:
497:
311:Pseudopseudohypoparathyroidism
1:
316:
1464:Autosomal dominant disorders
280:
250:
243:cells only express maternal
230:
7:
534:Cooper, Geoffrey M (2000).
335:of the 20th edition of
304:
207:
179:Hypoplasia of dental enamel
154:Choroid plexus(bottom left)
130:, and is classified as the
87:Gs alpha subunit deficiency
10:
1495:
1335:Legg–Calvé–Perthes disease
621:"Pseudohypoparathyroidism"
560:Reference, Genetics Home.
288:
247:(variant form of a gene).
18:
1403:
1377:
1320:
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1303:Osteochondritis dissecans
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454:Dermatology: 2-Volume Set
427:Kliegman, Robert (2016).
109:
101:
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83:
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53:
45:
36:
31:
1347:Osgood–Schlatter disease
1253:Relapsing polychondritis
1125:Osteonecrosis of the jaw
952:Osteitis fibrosa cystica
136:pseudohypoparathyroidism
21:McCune–Albright syndrome
1063:Paget's disease of bone
1014:Vertebral osteomyelitis
566:Genetics Home Reference
388:Kottler, Marie (2004).
913:Bone and joint disease
538:. Sinauer Associates.
155:
1393:Scheuermann's disease
1269:Slipping rib syndrome
1091:Hajdu–Cheney syndrome
153:
1186:Aneurysmal bone cyst
1142:Nonossifying fibroma
663:10.1136/adc.50.8.656
366:on 11 February 2017
237:signal transduction
188:Hypocalcemic tetany
140:parathyroid hormone
1418:Kienböck's disease
1174:Skeletal fluorosis
1120:Avascular necrosis
722:. Academic Press.
214:genetic imprinting
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146:Signs and symptoms
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1281:
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1157:Fibrous dysplasia
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1021:
850:
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562:"What is a gene?"
463:978-1-4160-2999-1
438:978-1-4557-7566-8
266:, phosphorus, PTH
259:Clinical features
121:
120:
93:Diagnostic method
26:Medical condition
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1384:
1352:Blount's disease
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1101:Gorham's disease
1068:Hypophosphatasia
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1367:Sever's disease
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1295:Osteochondritis
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1274:Tietze syndrome
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1248:Costochondritis
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1217:Pycnodysostosis
1152:Stress fracture
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1078:Bone resorption
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295:Fuller Albright
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116:Fuller Albright
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1469:Genodermatoses
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1205:Osteosclerosis
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657:(8): 656–658.
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982:Osteomyelitis
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176:calcification
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168:Brachydactyly
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60:Endocrinology
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22:
1405:
1379:
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1193:Hyperostosis
1178:
1058:Osteomalacia
1041:Osteoporosis
1036:Bone density
999:Sesamoiditis
969:
939:
930:Inflammation
871:
870:
869:profile for
866:
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823:
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793:
761:. Retrieved
746:
733:. Retrieved
718:
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629:. Retrieved
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544:. Retrieved
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517:. Retrieved
508:
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408:. Retrieved
396:
368:. Retrieved
364:the original
340:
326:
320:
292:
284:
254:
241:Renal tubule
234:
227:deficiency.
211:
191:
163:Hypogonadism
157:
123:
122:
1167:Polyostotic
1009:Periostitis
957:Brown tumor
763:12 February
735:12 February
605:12 February
519:12 February
485:(1): 45–8.
479:Acta Biomed
198:metacarpals
111:Named after
48:inheritance
1453:Categories
1240:Chondritis
1162:Monostotic
1116:Ischaemia
1086:Osteolysis
1053:Osteopenia
992:Involucrum
987:Sequestrum
836:DiseasesDB
631:2017-02-12
576:2017-02-12
546:2024-06-26
410:2017-02-12
370:9 February
317:References
200:, rounded
1180:bone cyst
1028:Metabolic
971:infection
941:endocrine
281:Treatment
272:test for
251:Diagnosis
231:Mechanism
218:autosomal
132:phenotype
102:Treatment
55:Specialty
1287:Combined
1046:Juvenile
625:Archived
599:Archived
570:Archived
540:Archived
513:Archived
509:omim.org
491:16116826
401:Archived
397:Orphanet
333:page 798
305:See also
221:dominant
208:Genetics
170:syndrome
75:Symptoms
863:Scholia
672:1545541
289:History
264:calcium
245:alleles
1424:elbow
1414:wrist
1096:Ainhum
865:has a
830:103580
819:275.49
754:
726:
681:173244
679:
669:
489:
460:
435:
341:(1918)
262:Serum
202:facies
184:cheeks
84:Causes
62:
1381:spine
1358:foot
1342:tibia
1313:Child
1262:Other
1231:Joint
1110:Other
867:topic
841:10835
804:E20.1
404:(PDF)
393:(PDF)
331:from
270:Urine
182:Full
1406:arm:
1331:hip
1323:leg:
921:Bone
825:OMIM
814:9-CM
765:2017
752:ISBN
737:2017
724:ISBN
677:PMID
607:2017
521:2017
487:PMID
458:ISBN
433:ISBN
372:2017
274:cAMP
810:ICD
795:ICD
667:PMC
659:doi
134:of
1455::
839::
828::
817::
802::
799:10
675:.
665:.
655:50
653:.
649:.
623:.
597:.
593:.
568:.
564:.
511:.
507:.
483:76
481:.
419:^
399:.
395:.
380:^
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