|1.||Newaz, M: 1 article (07/2015)|
|2.||Begum, B N: 1 article (07/2015)|
|3.||Akhter, N: 1 article (07/2015)|
|4.||De Luca, Francesco: 1 article (05/2014)|
|5.||Suarez, Elizabeth: 1 article (05/2014)|
|6.||Shoar, Zohreh: 1 article (05/2014)|
|7.||Ganguly, Tapan: 1 article (05/2014)|
|8.||Anderson, Carol E: 1 article (05/2014)|
|9.||Ramakrishna,: 1 article (11/2013)|
|10.||Kotecha, Nikunj: 1 article (11/2013)|
|2.||Congenital Abnormalities (Deformity)
11/01/2013 - "All these anomalies form part of a syndrome complex called MURCS ASSOCIATION (Mullerian agenesis/aplasia, renal anomalies, and Cervicothoracic Somite deformities)."
01/01/2013 - "A combination of the congenital abnormalities, Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia, is defined as the MURCS association. "
01/01/2008 - "We delineate this disease by reporting on a 16-year-old patient showing the cardinal features of MURCS association accompanied by a persistent left superior vena cava and atrial septal defect, orofacial clefting, and mild reduction deformities of the left hand. "
01/01/2011 - "This differential diagnosis includes (but is not limited to) Baller-Gerold syndrome, CHARGE syndrome, Currarino syndrome, deletion 22q11.2 syndrome, Fanconi anemia, Feingold syndrome, Fryns syndrome, MURCS association, oculo-auriculo-vertebral syndrome, Opitz G/BBB syndrome, Pallister-Hall syndrome, Townes-Brocks syndrome, and VACTERL with hydrocephalus. "
09/01/2008 - "This article provides a comprehensive review of the syndromes and disorders associated with NTDs, including Pallister-Hall syndrome, Walker-Warburg syndrome and Fukuyama congenital muscular dystrophy, MURCS association, Roberts syndrome, cerebro-costo-mandibular syndrome, laterality sequences, hydrolethalus syndrome, Knobloch syndrome, oculoauriculovertebral spectrum (hemifacial microsomia), cervico-oculo-acoustic syndrome, Fanconi anemia, Miller-Dieker lissencephaly syndrome, Fraser syndrome, frontonasal dysplasia, Adams-Oliver syndrome, CHILD syndrome, dyssegmental dysplasia, and monozygotic twinning. "
07/01/2015 - "Although there is a broad spectrum of anomalies described with MURCS association genitourinary fistula is not yet reported and reviewed in published articles. "
07/01/2015 - "We report on a 22 years old lady with aplasia of uterus and most of the vagina with normal secondary sexual characteristics, unilateral renal hypoplasia and anomalies of cervico throacic somites (MURCS Association), growth retardation, cardiac defect and congenital urethrovaginal fistula. "
02/01/2003 - "MURCS association and rectovestibular fistula: case report of a patient treated with one-stage posterior sagittal anorectoplasty and sigmoid loop vaginoplasty."
02/01/2003 - "Physical and radiologic examination of the patient found MURCS association with anorectal malformation (ARM) of rectovestibular-type fistula. "
|5.||Encephalocele (Encephalocele, Frontal)
01/01/2000 - "This is the second report of encephalocele with MURCS association."
01/01/2000 - "This fetus had the features of MURCS association with occipital encephalocele. "
01/01/2000 - "MURCS association with encephalocele: report of a second case."
01/02/1996 - "Occipital encephalocele and MURCS association: case report and review of central nervous system anomalies in MURCS patients."
01/02/1996 - "The combination of MURCS association (Müllerian duct and renal agenesis, upper limb and rib anomalies) and occipital encephalocele occurred in a stillborn girl of 41 weeks gestation. "
|1.||Hereditary renal agenesis
|2.||Adams Oliver syndrome