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Meigs' syndrome: Joe Vincent Meigs: gynecology: ascites with hydrothorax: Meigs' syndrome: the history of the eponym: Triad of ascites, hydrothorax and benign ovarian tumor Mellinghoff's sign: Karl Hermann Mellinghoff, German Endocrinologist, (1908–1967) hyperbaric medicine: cutaneous decompression sickness
Turner syndrome (TS), commonly known as 45,X, or 45,X0, [note 1] is a chromosomal disorder in which female cells have only one X chromosome instead of two, or are partially missing an X chromosome (sex chromosome monosomy) leading to the complete or partial deletion of the pseudoautosomal regions (PAR1, PAR2) in the affected X chromosome.
Wilson–Mikity syndrome; Wilson–Turner syndrome; Winchester syndrome; Winter-over syndrome; Wiskott–Aldrich syndrome; Wissler's syndrome; Withdrawal syndrome; Withering abalone syndrome; Wobbly hedgehog syndrome; Wolcott–Rallison syndrome; Wolff–Parkinson–White syndrome; Wolfram syndrome; Wolf–Hirschhorn syndrome; Woodhouse ...
Otherwise a physical examination may be carried out, and a medical history taken. Further diagnostic medical tests such as blood tests, scans, and biopsies, may be needed. An X-ray for example would soon be diagnostic of a suspected bone fracture. A noted significance detected during an examination or from a medical test may be known as a ...
Grey Turner's sign refers to bruising of the flanks, the part of the body between the last rib and the top of the hip. The bruising appears as a blue discoloration, [ 1 ] and is a sign of retroperitoneal hemorrhage , or bleeding behind the peritoneum, which is a lining of the abdominal cavity.
Turner syndrome [2] Poroma: Schöpf–Schulz–Passarge syndrome Clouston syndrome: Spiradenoma: Brooke–Spiegler syndrome: Fibrofolliculoma: Birt–Hogg–Dubé syndrome: Clear cell acanthoma: Ichthyosis: Acrochordon: Birt–Hogg–Dubé syndrome: Epidermal inclusion cyst with pilomatrical differentiation: Gardner's syndrome: Gardner fibroma
n/a Ensembl ENSG00000185960 n/a UniProt O15266 n/a RefSeq (mRNA) n/a n/a RefSeq (protein) NP_000442 NP_006874 n/a Location (UCSC) n/a n/a PubMed search n/a Wikidata View/Edit Human The short-stature homeobox gene (SHOX), also known as short-stature-homeobox-containing gene, is a gene located on both the X and Y chromosomes, which is associated with short stature in humans if mutated or present ...
Turner syndrome is an intersex condition wherein a person is born phenotypically female but with only one X chromosome or with X/XX mosaicism instead of XX or XY chromosomes. One study found that 23% of girls with Turner syndrome who were included met criteria for a diagnosis of an autism spectrum disorder and the majority had "significant ...