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Empty sella syndrome is the condition when the pituitary gland shrinks or becomes flattened, filling the sella turcica with cerebrospinal fluid instead of the normal pituitary. [2] It can be discovered as part of the diagnostic workup of pituitary disorders, or as an incidental finding when imaging the brain.
The empty sella sign occurs due to herniation of the subarachnoid space into the sella turcica, displacing the pituitary gland and allowing CSF to occupy the space. [3] This phenomenon is often linked to the following mechanisms: [4] Primary empty sella syndrome occurs without an underlying cause or pituitary pathology. It is associated with a ...
The various signs and symptoms in Sheehan's syndrome are caused by damage to the pituitary, thereby causing a decrease in one or more of the hormones it normally secretes. Since the pituitary controls many glands in the endocrine system , partial or complete loss of a variety of functions may result. [ 5 ]
Ectrodactyly–ectodermal dysplasia–cleft syndrome; Edwards syndrome; EEM syndrome; Egg drop syndrome; Ehlers–Danlos syndrome; Eiken syndrome; Einstein syndrome; Eisenmenger's syndrome; Eldomery-Sutton syndrome; Elejalde syndrome; Ellis–van Creveld syndrome; Emanuel syndrome; Empty nest syndrome; Empty nose syndrome; Empty sella syndrome
ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases. [ 1 ]
XLP syndrome X-linked lymphoproliferative syndrome (see Duncan Disease) XLSA X-linked sideroblastic anemia: XMEA X-linked myopathy with excessive autophagy: XMEN X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia XP Xeroderma pigmentosa: XSCID X-linked severe combined immunodeficiency: XXX syndrome ...
Affected infants appear normal at birth but may develop symptoms during the first year of life. Individuals with Salla disease may present with nystagmus as well as hypotonia, and may have difficulty coordinating voluntary movements (), reduced muscle tone and strength, and cognitive impairment. [5]
Patients with arachnoid cysts may never show symptoms, even in some cases where the cyst is large. Therefore, while the presence of symptoms may provoke further clinical investigation, symptoms independent of further data cannot—and should not—be interpreted as evidence of a cyst's existence, size, location, or potential functional impact on the patient.