Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance

Author:

Jones Kelly L.12ORCID,McNamara Erin A.3,Longoni Mauro4,Miller Danny E.5,Rohanizadegan Mersedeh6,Newman Laura A.7,Hayes Frances8,Levitsky Lynne L.9,Herrington Betty L.7,Lin Angela E.3

Affiliation:

1. Division of Medical Genetics and Metabolism; Children's Hospital of The King's Daughters; Norfolk Virginia

2. Department of Pediatrics; Eastern Virginia Medical School; Norfolk Virginia

3. Genetics Unit; MassGeneral Hospital for Children; Boston Massachusetts

4. Pediatric Surgical Research Laboratories; Massachusetts General Hospital; Boston Massachusetts

5. Department of Pediatrics; Seattle Children's Hospital, University of Washington; Seattle Washington

6. Division of Genetics and Genomics; Boston Children's Hospital, Harvard Medical School; Boston Massachusetts

7. Division of Pediatric Hematology/Oncology, Department of Pediatrics; University of Mississippi; Jackson Mississippi

8. Department of Medicine, Reproductive Endocrinology; Massachusetts General Hospital; Boston Massachusetts

9. Pediatric Endocrinology; MassGeneral Hospital for Children; Boston Massachusetts

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference146 articles.

1. Axenfeld-Rieger spectrum in a patient with 45,X Turner syndrome;Abdalla;Ophthalmic Genetics,2012

2. Turner's syndrome and hypogonadotrophic hypogonadism: Thalassemia major and hemochromatosis;Afonso Lopes;Journal of Pediatric Endocrinology and Metabolism,1995

3. Duchenne's muscular dystrophy in a girl with 45,X/46,XX chromosomal mosaicism;Aver'ianov;Zhrunal Nevropatologii I Psikhiatrii Imeni S. S. Korsakova,1977

4. Un nuevo tipo de aberracíon cromosómica: El mosaico normal/trisomia G-monosomia XO;Baguena Candela;Medicina Espanola,1965

5. Un caso con estigmas del síndrome de Bonnevie-Ullrich y del mongolismo y cariotipo 45, XO-trisomia G;Baguena Candela;Medicina Espanola,1966

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