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Familial Cushing's syndrome due to primary pigmented nodular adrenocortical disease. Reinvestigation 50 years later. 1989

W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Division of Endocrinology, Metabolism, and Internal Medicine, Mayo Clinic, Rochester, Minn 55905.

UI MeSH Term Description Entries
D007136 Immunoglobulins Multi-subunit proteins which function in IMMUNITY. They are produced by B LYMPHOCYTES from the IMMUNOGLOBULIN GENES. They are comprised of two heavy (IMMUNOGLOBULIN HEAVY CHAINS) and two light chains (IMMUNOGLOBULIN LIGHT CHAINS) with additional ancillary polypeptide chains depending on their isoforms. The variety of isoforms include monomeric or polymeric forms, and transmembrane forms (B-CELL ANTIGEN RECEPTORS) or secreted forms (ANTIBODIES). They are divided by the amino acid sequence of their heavy chains into five classes (IMMUNOGLOBULIN A; IMMUNOGLOBULIN D; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M) and various subclasses. Globulins, Immune,Immune Globulin,Immune Globulins,Immunoglobulin,Globulin, Immune
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009232 Myxoma A benign neoplasm derived from connective tissue, consisting chiefly of polyhedral and stellate cells that are loosely embedded in a soft mucoid matrix, thereby resembling primitive mesenchymal tissue. It occurs frequently intramuscularly where it may be mistaken for a sarcoma. It appears also in the jaws and the skin. (From Stedman, 25th ed) Angiomyxoma,Angiomyxomas,Myxomas
D009303 Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. Cancer of Nasopharynx,Nasopharyngeal Cancer,Cancer of the Nasopharynx,Nasopharynx Cancer,Nasopharynx Neoplasms,Neoplasms, Nasopharyngeal,Cancer, Nasopharyngeal,Cancer, Nasopharynx,Cancers, Nasopharyngeal,Cancers, Nasopharynx,Nasopharyngeal Cancers,Nasopharyngeal Neoplasm,Nasopharynx Cancers,Nasopharynx Neoplasm,Neoplasm, Nasopharyngeal,Neoplasm, Nasopharynx,Neoplasms, Nasopharynx
D009442 Neurilemmoma A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp964-5) Neurinoma,Schwannoma,Schwannomatosis, Plexiform,Neurilemoma,Neurilemmomas,Neurilemomas,Neurinomas,Plexiform Schwannomatoses,Plexiform Schwannomatosis,Schwannomas
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D010859 Pigmentation Disorders Diseases affecting PIGMENTATION, including SKIN PIGMENTATION. Incontinentia Pigmenti Achromians,Ito Syndrome,Schamberg's Disease,Schamberg Disease,Disease, Schamberg,Disease, Schamberg's,Disorder, Pigmentation,Disorders, Pigmentation,Pigmentation Disorder,Schambergs Disease,Syndrome, Ito
D003480 Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. Cushing's Syndrome,Hypercortisolism,Syndrome, Cushing,Syndrome, Cushing's
D004200 Diseases in Twins Disorders affecting TWINS, one or both, at any age. Diseases in Twin,Twin, Diseases in,Twins, Diseases in,in Twin, Diseases,in Twins, Diseases

Related Publications

W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
[A girl with Cushing's syndrome due to primary pigmented nodular adrenocortical disease].
October 2006, Nederlands tijdschrift voor geneeskunde,
W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Carney complex, a familial Cushing's syndrome due to primary pigmented nodular adrenocortical disease: a case report.
December 2002, The Kaohsiung journal of medical sciences,
W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Primary pigmented nodular adrenocortical disease and Cushing's syndrome.
November 2007, Arquivos brasileiros de endocrinologia e metabologia,
W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Cushing's syndrome resulting from primary pigmented nodular adrenocortical disease.
October 1986, American journal of diseases of children (1960),
W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Cushing's syndrome due to primary pigmented nodular adrenocortical disease with cardiac myxomas and mucocutaneous lentigines.
January 1992, Acta paediatrica (Oslo, Norway : 1992),
W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Familial Cushing's syndrome due to pigmented multinodular adrenocortical dysplasia.
March 1983, Acta endocrinologica,
W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease.
September 2002, The Journal of clinical endocrinology and metabolism,
W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Cushing's syndrome due to primary pigmented nodular adrenocortical disease--a case report reviews of the literature.
January 1995, The Korean journal of internal medicine,
W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Familial Cushing's syndrome with primary adrenocortical microadenomatosis (primary adrenocortical nodular dysplasia).
August 1980, Acta endocrinologica,
W F Young, and J A Carney, and B U Musa, and N M Wulffraat, and J W Lens, and H A Drexhage
Familial Cushing's syndrome due to nodular adrenocortical dysplasia. A putative receptor-antibody disease?
March 1986, Clinical endocrinology,
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