相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。CLOVES syndrome: review of a PIK3CA-related overgrowth spectrum (PROS)
A. Martinez-Lopez et al.
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Nephroblastomatosis or Wilms tumor in a fourth patient with a somatic PIK3CA mutation
Karen W. Gripp et al.
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Lymphatic and Other Vascular Malformative/Overgrowth Disorders Are Caused by Somatic Mutations in PIK3CA
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PIK3CA-Related Overgrowth Spectrum (PROS): Diagnostic and Testing Eligibility Criteria, Differential Diagnosis, and Evaluation
Kim M. Keppler-Noreuil et al.
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Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum
Kim M. Keppler-Noreuil et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2014)
Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome
Kyle C. Kurek et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Complex Spinal-Paraspinal Fast-Flow Lesions in CLOVES Syndrome: Analysis of Clinical and Imaging Findings in 6 Patients
A. I. Alomari et al.
AMERICAN JOURNAL OF NEURORADIOLOGY (2011)
Management of Combined Vascular Malformations
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Differential Diagnosis of Lower Extremity Enlargement in Pediatric Patients Referred with a Diagnosis of Lymphedema
Carolyn C. Schook et al.
PLASTIC AND RECONSTRUCTIVE SURGERY (2011)
Hermann Friedberg's case report: an early description of CLOVES syndrome
A. I. Alomari et al.
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CLOVES syndrome with thoracic and central phlebectasia: Increased risk of pulmonary embolism
Ahmad I. Alomari et al.
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The Misnomer “Macrocephaly–Cutis Marmorata Telangiectatica Congenita Syndrome”
Dakara Rucker Wright et al.
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Characterization of a distinct syndrome that associates complex truncal overgrowth, vascular, and acral anomalies: a descriptive study of 18 cases of CLOVES syndrome
Ahmad I. Alomari
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Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia
Carol L Clericuzio et al.
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Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi (CLOVE) Syndrome: CNS Malformations and Seizures may be a Component of This Disorder
Zoran S. Gucev et al.
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Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients
Julie C. Sapp et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice
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Giant fetal axillo-thoracic cystic hygroma associated with ipsilateral foot anomalies
Mehmet H. Atalar et al.
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Risk of tumorigenesis in overgrowth syndromes: A comprehensive review
P Lapunzina
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Wilms tumor screening is unnecessary in Klippel-Trenaunay syndrome
AK Greene et al.
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Characteristics and outcome of children with Beckwith-Wiedemann syndrome and Wilms' tumor: A report from the National Wilms Tumor Study Group
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