Results 371 to 380 of about 661,169 (403)
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Congenital adrenal hyperplasia
Medicine, 1990Congenital adrenal hyperplasia (CAH) results from enzymatic defects in the pathways of adrenal steroidogenesis, with over 90% of cases being due to 21-hydroxylase deficiency caused by autosomal recessive mutations in the CYP21 gene. Classical presentation—this is in the neonatal period with ambiguous genitalia/virilization of a female ...
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Congenital Adrenal Hyperplasia
New England Journal of Medicine, 1987Congenital adrenal hyperplasia is a group of autosomal recessive disorders resulting from the deficiency of one of the enzymes required for cortisol synthesis in the adrenal cortex.
Phyllis W. Speiser +2 more
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Cutaneous Lymphoid Hyperplasias
Seminars in Cutaneous Medicine and Surgery, 2000Benign hyperplastic lymphoid infiltrates of the skin (pseudolymphoma, older term) simulate lymphoma clinically and histologically. They can be divided into B-cell predominant (typical cutaneous lymphoid hyperplasia (CLH), angiolymphoid hyperplasia, Kimura's disease, and Castleman's disease) and T-cell predominant (T-cell CLH, lymphomatoid contact ...
Gary S. Wood, Anita C. Gilliam
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CONGENITAL ADRENAL HYPERPLASIA [PDF]
Endocrinology and Metabolism Clinics of North America, 1997 A clinical spectrum, varying from prenatal onset to postnatal onset of symptoms, exists in all hyperandrogenic forms of congenital adrenal hyperplasia (CAH). Postnatal onset hyperandrogenic symptoms such as premature pubarche, clitoromegaly, hirsutism, menstrual disorders and infertility are well known manifestations of CAH due to 21-hydroxylase ...
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Pseudoangiomatous stromal hyperplasia [PDF]
International Journal of Angiology, 2002 This report describes five cases of pseudoangiomatous stromal hyperplasia of the breast. The lesion manifested as a discrete palpable slowly growing lumps. The patients ranged in age from 30 to 71 years. The clinical diagnosis was that of fibroadenoma in most cases.
Jasim Radhi, Ed Alport
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Pathology - Research and Practice, 1988
The morphologic study of a large number of human pituitary tissues provided conclusive evidence that hyperplasia of various adenohypophysial cell types exists. These rare lesions may serve as the underlying cause of pituitary hypersecretory syndromes.
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The morphologic study of a large number of human pituitary tissues provided conclusive evidence that hyperplasia of various adenohypophysial cell types exists. These rare lesions may serve as the underlying cause of pituitary hypersecretory syndromes.
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Hyperplasia of lymphatic vessels in VEGF-C transgenic mice.
Science, 1997No growth factors specific for the lymphatic vascular system have yet been described. Vascular endothelial growth factor (VEGF) regulates vascular permeability and angiogenesis, but does not promote lymphangiogenesis.
M. Jeltsch +9 more
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Hyperplasia of the Coronoid Process
Asian Journal of Oral and Maxillofacial Surgery, 2006Abstract Objective: To review the morphology, aetiology, clinical symptoms, diagnosis, and therapy of true coronoid hyperplasia. Patients and Methods: The record of all patients with a confirmed diagnosis of mandibular coronoid hyperplasia presenting to the Department of Oral and Maxillofacial Surgery, University of Bonn, Bonn, Germany, between 1995
Wenghoefer, M.H. +5 more
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Congenital Adrenal Hyperplasia
AJN, American Journal of Nursing, 1976The child with congenital adrenal hyperplasia can lead a normal life provided the diagnosis is made early. But daily adjustment of medication makes up the day of families whose children have this genetically determined condition. Although uncommon statistically, the condition poses real problems to the parents and staff who manage the child's health ...
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