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Find link is a tool written by Edward Betts.Longer titles found: Pseudohypoparathyroidism (view), X-linked recessive hypoparathyroidism (view), Pseudopseudohypoparathyroidism (view)
searching for Hypoparathyroidism 27 found (117 total)
alternate case: hypoparathyroidism
Kenny-Caffey syndrome
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(unlike KCS2), and is also known as the Sanjad-Sakati syndrome or Hypoparathyroidism-Retardation-Dysmorphism Syndrome. Kenny-Caffey syndrome type 2 isAcrodysostosis (588 words) [view diff] exact match in snippet view article find links to article
fusing Scoliosis Pain – joint, hip, lower back, wrist Hypothyroidism Hypoparathyroidism Pseudohypoparathyroidism Vitamin D deficiency Thyroid cysts Type 1Riedel's thyroiditis (616 words) [view diff] exact match in snippet view article find links to article
hoarseness. Patients may present with symptoms of hypothyroidism and hypoparathyroidism as the gland is replaced by Fibrous tissues . Physical examinationTBCE (849 words) [view diff] exact match in snippet view article find links to article
and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM intervalGCM2 (535 words) [view diff] exact match in snippet view article find links to article
Schubert SW, Parma J, et al. (2005). "GCMB mutation in familial isolated hypoparathyroidism with residual secretion of parathyroid hormone". J. Clin. EndocrinolTrousseau sign of latent tetany (322 words) [view diff] exact match in snippet view article find links to article
OA; Calverley, JR (August 1967). "Neurological manifestations of hypoparathyroidism". Archives of Internal Medicine. 120 (2): 202–6. doi:10.1001/archinte1968 in science (1,145 words) [view diff] exact match in snippet view article find links to article
thymus and its immunologic consequences: concurrence with congenital hypoparathyroidism, vol. IV, White Plains, NY: March of Dimes-Birth Defects FoundationDevelopment of the endocrine system (3,139 words) [view diff] exact match in snippet view article find links to article
DiGeorge-like syndrome. Malformations in the GCM2 gene have resulted in hypoparathyroidism. Studies on SOX3 gene mutations have demonstrated that it plays aImmunodeficiency (1,810 words) [view diff] exact match in snippet view article find links to article
infections coexist: organ-specific autoimmune manifestations (e.g., hypoparathyroidism and adrenocortical failure) and chronic mucocutaneous candidiasisHypodontia (7,611 words) [view diff] exact match in snippet view article find links to article
between systemic diseases, endocrine disruption (i.e. idiopathic hypoparathyroidism and pseudohypoparathyroidism) and ectodermal dysplasia. However, aEndocrine system (4,579 words) [view diff] exact match in snippet view article find links to article
DiGeorge-like syndrome. Malformations in the GCM2 gene have resulted in hypoparathyroidism. Studies on SOX3 gene mutations have demonstrated that it plays aInferior thyroid artery (707 words) [view diff] exact match in snippet view article find links to article
thyroid artery accidental ligation during thyroidectomy can cause hypoparathyroidism. The injection of dye into the inferior thyroid artery can be usedSyndromes affecting the heart (113 words) [view diff] exact match in snippet view article find links to article
tetralogy of Fallot Craniofacial Thymic aplasia Cleft palate Hypocalcemia/hypoparathyroidism Acute coronary syndrome Commonly associated with three clinical manifestations:Splice site mutation (1,719 words) [view diff] exact match in snippet view article find links to article
the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism". Nature Genetics. 1 (2): 149–152. doi:10.1038/ng0592-149. PMID 1302009Andrea Superti-Furga (2,272 words) [view diff] exact match in snippet view article find links to article
Ekkehart; Magnani, Cinzia (June 2013). "FAM111A Mutations Result in Hypoparathyroidism and Impaired Skeletal Development". The American Journal of HumanCalcium-sensing receptor (4,087 words) [view diff] exact match in snippet view article find links to article
Ca(2+)-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism". Human Molecular Genetics. 5 (5): 601–6. doi:10.1093/hmg/5.5.601Angelo DiGeorge (954 words) [view diff] exact match in snippet view article find links to article
thymus and its immunologic consequences: concurrence with congenital hypoparathyroidism. IV(1). White Plains, NY: March of Dimes-Birth Defects Foundation;Chronaxie (2,365 words) [view diff] exact match in snippet view article find links to article
neuromuscular junction diseases. Chronaxie is increased in the tetany of hypoparathyroidism. It must be remembered, however, that it is the rheobase which correspondsAutoimmunity (5,573 words) [view diff] exact match in snippet view article find links to article
infections coexist: organ-specific autoimmune manifestations (e.g., hypoparathyroidism and adrenocortical failure) and chronic mucocutaneous candidiasisAbaloparatide (1,919 words) [view diff] exact match in snippet view article find links to article
delivery of parathyroid hormone and its analogues for osteoporosis and hypoparathyroidism - translating the pharmacology". British Journal of Clinical PharmacologyHouse mouse (7,615 words) [view diff] exact match in snippet view article find links to article
Natasha; Karaplis, Andrew C. (2001). "Genetics and animal models of hypoparathyroidism". Trends in Endocrinology & Metabolism. 12 (7). Cell Press: 288–294Thalassemia (6,592 words) [view diff] exact match in snippet view article find links to article
gonadotrophin secretion which leads to delayed, slow or arrested puberty. 2) Hypoparathyroidism: chronic anemia causes hematopoiesis which results in bone reabsorptionDevaka Fernando (2,336 words) [view diff] exact match in snippet view article find links to article
1016/S0140-6736(13)61905-4. PMID 24139977. S2CID 35941804. "First Hypoparathyroidism Awareness meeting". btfthyroid.org. Retrieved 1 September 2011. "JointThymic epithelial cell (1,409 words) [view diff] exact match in snippet view article find links to article
APECED (APS-1), which is manifested by mucocutaneous candidiasis, hypoparathyroidism and adrenal insufficiency. There are many autoimmune diseases, causedList of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article
612949; SLC25A12 Hypoparathyroidism, autosomal dominant; 146200; PTH Hypoparathyroidism, autosomal recessive; 146200; PTH Hypoparathyroidism, familial isolated;Chemotherapy (17,494 words) [view diff] exact match in snippet view article find links to article
are found in the blood. High levels of phosphate induce secondary hypoparathyroidism, resulting in low levels of calcium in the blood. This causes kidneyGluten-sensitive enteropathy–associated conditions (7,556 words) [view diff] exact match in snippet view article find links to article
PMID 9689318. Wortsman J, Kumar V (1994). "Case report: idiopathic hypoparathyroidism co-existing with coeliac disease: immunologic studies". Am. J. Med