Article citationsMore>>

Kurek, K.C., Luks, V.L., Ayturk, U.M., Alomari, A.I., Fishman, S.J., Spencer, S.A., et al. (2012) Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome. The American Journal of Human Genetics, 90, 1108-1115.
https://doi.org/10.1016/j.ajhg.2012.05.006

has been cited by the following article:

• TITLE: Cloves Syndrome: A Case Series of a Rare Syndrome

  AUTHORS: Warigbani Pieterson, Edem Anyigba, Omane Acheamfour Okrah, Hafisatu Gbadamosi, Elleisabeth Pieterson

  KEYWORDS: Overgrowth Syndrome, CLOVES, Vascular Anomalies, Clinical Symptomatology, Imaging Spectrum

  JOURNAL NAME: Modern Plastic Surgery, Vol.16 No.1, January 29, 2026

  ABSTRACT: “Overgrowth” syndrome generally describes abnormal growth patterns in the milieu of a constellation of other symptoms and signs. CLOVES (Congenital Lipomatous asymmetric overgrowth of the trunk with lymphatic, capillary, venous and combined-type vascular malformations, epidermal naevi, scoliosis/ skeletal and spinal anomalies) is a segmental overgrowth syndrome with vascular anomalies. The clinical symptomatology is thus very variable and based on the involved systems. This groundbreaking series seeks to document the clinical and imaging spectrum of findings in these four children, which will be the first of its kind in Ghana, West Africa.