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syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Virchow-Seckel syndrome — (also known as bird headed dwarfism, Harper s syndrome or Seckel dwarfism) is a syndrome of unknown etiology, characterized by intrauterine growth retardation and postnatal dwarfism with a small head, narrow bird like face with a beak like nose,… … Wikipedia
Hypermobility — Classification and external resources [[File: |frameless|upright=1.06|alt=]] Hypermobile fingers and thumb ICD 10 M35.7 … Wikipedia
Seckel syndrome — Classification and external resources ICD 10 Q87.1 OMIM 210600 DiseasesDB … Wikipedia
Koo-Koo the Bird Girl — Koo Koo, the Bird Girl was born Minnie Woolsey in 1880. When she died is unknown, but accounts show that she was still alive in 1960. Woolsey suffered from a rare skeletal disorder called Virchow Seckel syndrome, which caused her to have a very… … Wikipedia
Bannayan syndrome — A genetic disease characterized by macrocephaly (enlarged head), multiple lipomas (benign fatty tumors) and hemangiomas (benign blood vessel tumors). The macrocephaly occurs without enlargement of the cerebral ventricles. There is mild… … Medical dictionary
Gigantism — refers to excessive growth both in height and specific body parts. Gigantism with extreme growth in height may be associated with disorders of the pituitary gland, which secretes human growth hormone (somatotrophin) during childhood before the… … Medical dictionary
Macrocephaly, multiple lipomas, and hemangiomas — Bannayan syndrome, a genetic disease characterized by macrocephaly (enlarged head), multiple lipomas (benign fatty tumors) and hemangiomas (benign blood vessel tumors). The macrocephaly occurs without enlargement of the cerebral ventricles. There … Medical dictionary
Franceschetti–Klein syndrome — Classification and external resources ICD 9 756.0 OMIM 154500 DiseasesDB … Wikipedia
mandibulofacial dysostosis — man·di·bu·lo·fa·cial dysostosis man .dib yə lō .fā shəl n a dysostosis of the face and lower jaw inherited as an autosomal dominant trait and characterized by bilateral malformations, deformities of the outer and middle ear, and a usu. smaller… … Medical dictionary
