Results 221 to 230 of about 615,013 (286)

Caudal duplication syndrome in a young girl: Gastrointestinal and genitourinary duplication with spinal dysraphism. [PDF]

Urol Case Rep
Saleem M, Saleem U, Basit A, Saleem A, Butt J, Ali A, Sher Khan MQ, Dawood AB, Talat N, Imran A.   +9 more
europepmc   +1 more source

Anesthetic Management of Cesarean Delivery in a Patient With Ellis-van Creveld Syndrome. [PDF]

J Med Cases
Kalvapudi D, Shah SA, Singh H.
europepmc   +1 more source

Filamin B (<i>FLNB</i>)-Related Spondylocarpotarsal Synostosis Syndrome: Systematic Literature Review and Novel Case Report. [PDF]

Genes (Basel)
Gobbetto C, Passarella S, Zoller T, Lanzafame R, Gaudino R, Ambrosetti I, Pietrobelli A, Antoniazzi F.   +7 more
europepmc   +1 more source

Skeletal Anomalies and Deformities in Patients With Deletions of 22q11

American Journal of Medical Genetics, Part A, 1997
Skeletal anomalies in patients with a 22q11.2 deletion are reported infrequently. We report the skeletal findings in 108 patients with a 22q11.2 deletion, of whom 37 (36%) had a skeletal anomaly. Twenty-two patients (20%) had anomalies of the limbs, 7 of the upper limb, including preaxial or postaxial polydactyly. An anomaly of the lower limb was found
Elaine Zackai, Beverly S Emanuel, Richard I Markowitz   +2 more
exaly   +5 more sources