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Mueller–Weiss syndrome, also known as Mueller–Weiss disease, is a rare [2] idiopathic degenerative disease of the adult navicular bone characterized by progressive collapse and fragmentation, leading to mid- and hindfoot pain and deformity. [3] [1] It is most commonly seen in females, ages 40–60. [4]
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 ...
Malformative syndrome; Mallory–Weiss syndrome; Malnutrition–inflammation complex; Malouf syndrome; Malpuech facial clefting syndrome; Management of chronic headaches; Manning criteria; Marchiafava–Bignami disease; Marden–Walker syndrome; Mare reproductive loss syndrome; Marfan syndrome; Marfanoid–progeroid–lipodystrophy syndrome ...
In 1929, Mallory and Soma Weiss, a physician at Harvard, reported on 15 cases of severe, painless hemorrhage caused by a tear in the mucosa of the esophagus or gastroesophageal junction preceded by vomiting in alcoholic patients. [3] They reported a further six cases in 1932. [4] This syndrome has become known as Mallory–Weiss syndrome.
A clinically isolated syndrome (CIS) is a clinical situation of an individual's first neurological episode, caused by inflammation or demyelination of nerve tissue. An episode may be monofocal , in which symptoms present at a single site in the central nervous system , or multifocal , in which multiple sites exhibit symptoms.
A syndrome is a set of medical signs and symptoms which are correlated with each other and often associated with a particular disease or disorder. [1] The word derives from the Greek σύνδρομον, meaning "concurrence". [2]: 1818 When a syndrome is paired with a definite cause this becomes a disease. [3]
Jackson–Weiss syndrome (JWS) is a genetic disorder characterized by foot abnormalities and the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face.
Urbach–Wiethe disease is very rare; there are fewer than 300 reported cases in medical literature. [2] Although Urbach–Wiethe disease can be found worldwide, almost a quarter of reported diagnoses are in South Africa. [2] Many of these are in patients of Dutch, German, and Khoisan ancestry.