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490 Possible Causes for Multiple Endocrine Neoplasia Type 2A

  • Medullary Thyroid Carcinoma

    To present an unusual case of multiple endocrine neoplasia type 2A (MEN 2A) syndrome and to describe how this case differs from the typical clinical features and usual genetic[ncbi.nlm.nih.gov] Endocrine Neoplasia Type 2a/genetics Multiple Endocrine Neoplasia Type 2a/pathology Proto-Oncogene Proteins c-ret/genetics Retrospective Studies Sensitivity and Specificity[ncbi.nlm.nih.gov] We present a case of choroidal metastasis as a first presentation of disease progression in a patient with Multiple Endocrine Neoplasia type 2A syndrome (MEN2A) who had undergone[ncbi.nlm.nih.gov]

  • Primary Hyperparathyroidism

    Inherited forms of primary hyperparathyroidism like Multiple Endocrine Neoplasia Type 1, Multiple Endocrine Neoplasia Type 2a, Hyperparathyroidism-Jaw Tumor Syndrome or isolated[ncbi.nlm.nih.gov] endocrine neoplasia type 2A.[ojrd.biomedcentral.com] The aim of this update is to review the clinicopathological features, genetic bases and current management for patients with PHPT associated with multiple endocrine neoplasia[ncbi.nlm.nih.gov]

  • Familial Medullary Thyroid Carcinoma

    We present the phenotype-genotype of 12 Greek families with multiple endocrine neoplasia type 2A (MEN 2A) or familial medullary thyroid carcinoma (FMTC).[ncbi.nlm.nih.gov] Abstract Multiple endocrine neoplasia type 2A (MEN2A) and familial medullary thyroid carcinoma (FMTC) are autosomal dominant inherited cancer syndromes with incomplete penetrance[ncbi.nlm.nih.gov] endocrine neoplasia type 2A (MEN 2A), familial medullary thyroid carcinoma (FMTC), or Hirschsprung's disease.[ncbi.nlm.nih.gov]

  • Pheochromocytoma

    Several hereditary susceptibility disorders are known to be associated with pheochromocytoma/paragangliomas such as multiple endocrine neoplasia type 2 (2A or B).[ncbi.nlm.nih.gov] A 45-year-old woman was diagnosed as having multiple endocrine neoplasia type 2A in 2014.[ncbi.nlm.nih.gov] One of these is multiple endocrine neoplasias type 2A and type 2B, where pheochromocytoma is caused by a mutation in the RET gene, which is a protooncogene that encodes for[osmosis.org]

  • Parathyroid Adenoma

    ., multiple endocrine neoplasia type 1 or type 2A, familial hyperparathyroidism) Parathyroid hormone–independent Renal failure, acute or chronic* Neoplasms Parathyroid hormone–related[aafp.org] endocrine neoplasia type 1 or type 2A, familial hyperparathyroidism) Parathyroid hormone–independent Renal failure, acute or chronic* Neoplasms Parathyroid hormone–related[aafp.org] […] protein dependent Osteolytic metastases and multiple myeloma Other humoral syndromes Excess vitamin D Ingested or topical vitamin D analogues Granulomatous disease Williams[aafp.org]

  • Multiple Endocrine Neoplasia

    CLINICAL CASE REPORT Pancreatitis as the first manifestation of multiple endocrine neoplasia type 2A Pancreatite como primeira manifestação de neoplasia endócrina múltipla[doi.org] Two distinct clinical forms have been described as the following phenotypes: multiple endocrine neoplasia type 2A (MEN 2A) and multiple endocrine neoplasia type 2B (MEN 2B[ncbi.nlm.nih.gov] Abstract The clinical characteristics and RET proto-oncogene (RET‑PO) mutation status of a patient with multiple endocrine neoplasia type 2A pedigree (MEN2A) was analyzed[ncbi.nlm.nih.gov]

  • Multiple Endocrine Neoplasia Type 2A

    MEN-2A syndrome Multiple Endocrine Neoplasia, Type II Multiple Endocrine Neoplasia Type II MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA MEN Type II MEN Type 2a Multiple Endocrine[wikidata.org] The presence of two of the neoplasms belonging to multiple endocrine neoplasia type 2A is enough to make a clinical diagnosis.[symptoma.com] Multiple endocrine neoplasia type 2A (MEN 2A) is an autosomal dominant inherited cancer syndrome that expresses nonendocrine and endocrine tumors.[ncbi.nlm.nih.gov]

  • Multiple Endocrine Neoplasia Type 2B

    Further information outlining the clinical features of Multiple Endocrine Neoplasia Type 2A and Type 2B.[eviq.org.au] Pheochromocytomas are identified in 50% of individuals with multiple endocrine neoplasia type 2A and multiple endocrine neoplasia type 2B.[doi.org] Multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and multiple endocrine neoplasia type 2B are collectively associated with a 70-100% risk of medullary[ncbi.nlm.nih.gov]

  • Multiple Endocrine Neoplasia Type 4

    endocrine neoplasia type 2A (MEN-2A).[link.springer.com] , MEN2a, Multiple Endocrine Neoplasia Type 2a, Multiple Endocrine Neoplasms Type 2a, Neoplasia, Multiple Endocrine Type 2a, Neoplasms, Multiple Endocrine Type 2a, MEN syndrome[fpnotebook.com] Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.[en.wikipedia.org]

  • Thyroid Cancer

    Endocrine Neoplasia types 2A and 2B.[california.providence.org] Genetic factors There are three hereditary forms: familial medullary thyroid carcinoma; multiple endocrine neoplasia type 2A (MEN-2A), characterized by medullary thyroid cancer[web.archive.org] .: Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363 (6428): 458-60, 1993.[web.archive.org]

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