WordNet

an abnormal condition in males in which the urethra opens on the under surface of the penis

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Toriello Carey syndrome: genetic, clinical, and oral considerations: a case report.

Maretti MB1, Haddad AS, Ferreira MC, Guaré Rde O, Alonso LG.
Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry.Spec Care Dentist.2011 Mar-Apr;31(2):68-72. doi: 10.1111/j.1754-4505.2011.00179.x.
Toriello Carey syndrome is a rare recessive autosomal disease whose clinical manifestations are more evident in males. Some authors report that the general characteristics of this disease are agenesis of the corpus callosum, mental disability, convulsions, atrial septal defect, pulmonary artery sten
PMID 21371068

Do patients with hypospadias and cryptorchidism share a common phenotype? Case-control study of an Italian paediatric population.

Marrocco G1, Bruner E, Vallasciani S, Majore S, Grammatico P.
Journal of pediatric urology.J Pediatr Urol.2007 Dec;3(6):477-9. doi: 10.1016/j.jpurol.2007.05.001. Epub 2007 Jun 27.
OBJECTIVE: A large number of children affected by hypospadias and undescended testis (UDT) are characterized facially by a large forehead with frontal bossing, telecanthus and broad flat nasal bridge. These traits are classically part of the clinical spectrum of the Opitz-GBBB and other syndromes. T
PMID 18947798

Battaglia A1, Chines C, Carey JC.
American journal of medical genetics. Part A.Am J Med Genet A.2006 Oct 1;140(19):2075-9.
Initially described as a rare MCA/MR syndrome occurring only in boys, due to a recessive mutation on the X chromosome [Opitz and Kaveggia, 1974], the FG syndrome (FGS) now emerges as a more common disorder also occurring in girls. Based on over 50 reported cases, FGS is associated with developmental
PMID 16691600

鈴木康之,岡成寛,北原倍,小野和郎,有馬正高
先天異常 : 日本先天異常学会会報 : official journal of Congeital Anomalies Research Association of Japan 15(4), 226, 1975-12-30
NAID 110002728657

英: Opitz syndrome
同: オピッツ・フリアス症候群 Opitz-Frias syndrome、両眼開離尿道下裂症 telecanthus hypospadias、Opitz oculo-genito-laryngeal syndrome

Opitz syndrome , Opitz-Frias syndrome a familial syndrome consisting of hypertelorism and hernias, and in males also characterized by hypospadias, cryptorchidism, and bifid scrotum. Cardiac, laryngotracheal, pulmonary, anal, and renal abnormalities may also be present.