You are here

PSÖDOHİPOPARATİROİDİZM TANILI VAKALARIMIZDA PTH TESTİ VE Gs PROTEİN DÜZEYİ İLE TİP TAYİNİ VE KLİNİK SEYİR İLE İLİŞKİSİ

Journal Name:

Publication Year:

Abstract (2. Language): 
Classification of pseudohypoparathyroidism with pth test and gs protein levels and coırelation witlı the ciinical coıırse. Pseudohypoparathyroidism (PHP), caused by decreased Gs protein acti-vity, is a rare disease which is characterised by parafhormone resistance. İn type 1 PHP, the defici-ency of other hormones which act by Gs protein can also be encountered. The patients, who were 3 months, 14 and 13,7 years old, presented with seizures, exhaustion and carpopedal spasm. Ca-se 1 also had extended jaundice and constipation. Case 2 and 3 had mild course facies on physical examination and case 3 had short 5lh metacarp. Case 2 and 3 had mental retardation and case 1 had mild motor retardation.» Ali three cases had hypocalcemia, hyperphosphatemia, increased alkaline phosphatase and parafhormone (PTH) levels. Case 3 had multıple calcification on compu-terized cranial tomography, Case 1 also had primary hypothyroidism. Diagnosis of PHP was confirmed in case 1 (typel ) and 2 (type 2) by PTH test. Gs protein activity was found low (70 %) (normal range: (85-110 %) in case 3, compatible with type 1 PHP . Case 2 had normal Gs protein activity in remission. The patients were put on calcium and active vitamine D therapy. Nephrocalcinosis was observed in the second year of therapy in case 2. Remission was encountered in case 1 and 2 and the therapy was discontinued. In conclusion, it is noteworthy that our patient with type 2 PHP had multiple hormone resistance which is frequently observed in typel PHP. Spontaneous remission may occur in the natural prog-ress of PHP for which patients should be checked at certain intervals.
Abstract (Original Language): 
Psödohipoparatiroidizm (PHP) parathormona doku yanıtsızhğına bağlı hipokalsemi, hiperfosfate-mi ile karakterize, parathormon vermekle bulgularının düzeltilemediği heterojen bir hastalık grubudur. Gs protein aktivitesinde düşüklük bulunan Tip la PHP'de Gs proteinin aracılık ettiği diğer hormonlara da direnç ortaya çıkabilmektedir. Kliniğimize konvülziyon geçirme, halsizlik, karpo-pedal spazm nedeniyle başvuran 3 erkek vaka (sırasıyla 3 ay, 14 yaş, 13.7 yaş) incelendi. Vaka l'in aynı zamanda uzamış sarılık ve kabızlık yakınması mevcuttu. Fizik muayenede hafif kaba yüz görünümü, vaka 3'de ayrıca ellerde 5.metakarp kısalığı dikkat çekiyordu. Vaka 1 hafif motor geriliğe vaka 2 ve 3 ise mental geriliğe sahipti. Hipokalsemi, hiperfosfatemi, alkali fosfataz ve parathormon yüksekliği mevcuttu. Vaka 3'de bilgisayarlı beyin tomografisinde yaygın kalsifikas-yon odakları gözlendi.. Vaka l'e ilave olarak primer hipotiroidi eşlik ediyordu.PTH testi ile vaka l'de tip 2, vaka 2'de ise tip 1 PHP tanısı kesinleşti. Gs protein aktivitesi vaka 3'de düşük (%70) (N:%85-110) ve tipi PHP ile uyumlu bulundu.Vaka 2'nin ise remisyon döneminde bakılabilen Gs protein aktivitesi normaldi. Vakaların hepsine kalsiyum ve aktif D vitamini, vaka l'e ilave olarak L-tiroksin yerine koyma tedavisi başlandı. Vaka 2'de izlemin 2.yılında nefrokalsinoz gelişti. Vaka 1 ve 2'de izlem sırasında (sırasıyla 3.5 ve 2.7 yıl) spontan düzelme gözlendi, aktif D vitamini tedavisine ihtiyaç kalmadı.. Psödohipoparatiroidizm tanılı vakalarda çoğul hormon direncinin tip 1 vakalarına eşlik ettiğinin bildirilmesine karşın, bizim tip 2 PHP tanılı vakamızda TSH direnci bulunması ve iki vakamızın izlem sırasında spontan düzelme göstermesi ilginç bulundu. Sonuç olarak PHP'li vakalarının çoğul hormon direncinin eşlik edebilmesi ve tedavi sırasında nefrokalsinoz gelişebilmesi gibi durumlar açısından yakından izlenmeleri gerekmektedir. Ayrıca PHP'li vakalarda PTH'ya yanıtsızlığın spontan olarak düzelebildiği akılda tutulmalıdır.
182-188

REFERENCES

References: 

1. Ahmet SF, Dixon PH, Bonthron DT, Stirling HF, Barr DGD, Kelnar CJH, Thakker RV: GNAS1 mutational analysis pseudohypoparathyroidism. Clin Endocrinol 49:525 (1998).
2. Amino N: Receptors in disease: An overview. Clinical Biochemistry, 23:31 (1990).
Psödohipoparatiroidizm Tandı Vakalarımızda PTH Testi ve Gs Protein Düzeyi ile Tip Tayini ve Klinik Seyir ile İlişkisi
3. Chan JCM, Young RB, Hartenberg MA, Chinchilli VM: Calcium and phosphate metabolism in children vvith idio-pathic hypoparathyroidism or pseudohypoparathyroidism : Effecls of 1,25 dihydroxyvitanıin D3. J Pediatr 106: 421 (1985).
4. Dabbagh S, Chesney RW, Langer LO, DeLuca HF, Gil-bert EF, Deweerd JH: Renal-nonresponsive, bone-res-ponsive pseudohypoparathyroidism. AJDC 138: 1030 (1984).
5. Farfel Z, Priedman E: Mental deficiency in pseudohypoparathyroidism type I is associated with Ns-protein deficiency. Ann Intern Med 105:197 (1986).
6. Foull CM, VVelbury RR, Paul B, Kendall-Taylor P: Pseudohypoparathyroidism : Its phenotypic variability and associaled disorders in a large family. Q J Med; 78:251 (1991).
7. Kaartinen JM, Kaar ML, Ohisalo JJ: Defective and sti-mulation of adipocyte adenylate cyclase, blunted lipoly-sis, and obesty in pseudohypoparathyroidism la. Pediatr Res 35: 594 (994).
8. Keır D, Hosking DJ: Pseudohypoparathyroidism: Clini-cal expression of PTH resistance. Q J Med; 65: 886 (1987).
9. Kruse K, Kracht U: A simplified diagnoslic test in hypo-parathroidism and pseudohypoparathyroidism type I vvith synthetic 1-38 fragment of human parathyroid hormone. EurJ Pediatr 146:373 (1987).
10. Levine MA, Jap TS, Hung W: Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type la. J Pediatr ; 107:919 (1985).
11. Levine MA, Jap TS, Mauseth RS, Dovvns RW, Spiegel AM: Activity of stimulatory guanine nucleotide-binding protein Is reduced in erythrocytes from patients with pseudohypoparathyroidism: Biochemical, endocrine, and genetic analysis of AIbright's hereditary osteodystrophy in six kindreds. J Clin Endocrinol Metab; 62: 497 (1986).
12. Levine MA, Moses AM, Breslau NA, Marx SJ, Lasker RD, Rizzoli RE, Aurbach GD, Spiegel AM: Resistance to multiple hormones in patients with pseudohypoparathyroidism. AmJ Med 74: 545 (1983).
13. Mantovani G, Romoli R, Weber G, De Menis E, Beccio S, Beck-Peccoz P, Spada A: Identification of t\vo novel mutations. J Clin Endocrinol Metab 85:4243 (2000).
14. Marguet C, Mallet E, Basuyau JP, Martin D, Leroy M, Brunelle P: Clinical and biological heterogeneity in pseudohypoparathyroidism syndrome. Horm Res 48:120 (1997).
15. Ringel MD, Schwindinger WF, Levine MA: Clinical implications of genetic defect in G proteins. The molectı-lar basis of Mc Cune-Albright syndrome and Albright Hereditary Osteodystrophy. Medicine 75:171 (1996).
16. Schuster V, Eschenhagen T, Kruser K, Gierschik P, Kreth HW: Endocrine and molecular biological studies in a German family vvith Albright hereditary osteodystrophy. Eur JPediatr, 152:185 ( 1993).
17. Silve C: Pseudohypoparathyroidism syndromes: the many faces of parathyroid hormone resistance. Eur J Endocrinol. 133:145 (1995).
18. Sohn HE, Furuka\va Y, Yumita S, Miura R, Unakami H, Yoshinaga K: Effect of 1-34 fragment of human parathyroid hormone on plasma adenosine 3',5'-monophoshate (cAMP) concentrations and the diagnostic criteria based no the plasma cAMP response in Ellsworth-Howard test. Endocrinol Japon 31:33(1984).
19. Yu Davven, Yu S, Schuster V, Kruse K, Clericuzio CL, Weinstein LS: Identification of two novel deletion mutations vvifhin the Gs( gene (GNAS1) in Albright hereditary osteodystrophy. J Clin Endocrinol Metab 84: 3254 (1999).
20. Weisinger JR, Mogollon A, Lander R, Bellorin-Font E, Riera R, Abadi I, Paz-Martinez V: Massive cerebral cal-cifications associated vvith increased renal phosplıate re-absoıption. Arch İntem Med 146: 437 (1986).

Thank you for copying data from http://www.arastirmax.com