Related Experiment Video
Updated: May 28, 2026

Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
Published on: March 23, 2022
Growth hormone deficiency: an unusual presentation of floating harbor syndrome
Assimina Galli-Tsinopoulou1, Ioannis Kyrgios, Eleftheria Emmanouilidou
1Fourth Department of Pediatrics, Medical School, Aristotle University of Thessaloniki, Papageorgiou General Hospital Thessaloniki, Greece. galtsin@otenet.gr
Abstract:
Floating-Harbor Syndrome (FHS) is a very rare condition of unknown etiology characterized by short stature, delayed bone age, characteristic facial features, delayed language skills and usually normal motor development. This syndrome has only once been associated with growth hormone deficiency and precocious puberty in the same patient. We describe a 5 4/12 year-old girl with the typical features of FHS in whom growth hormone deficiency was diagnosed and two years later central precocious puberty was noted. The patient showed a good response to human recombinant growth hormone as well as gonadotropin releasing hormone analogue treatment.
Related Concept Videos
Hyperosmolar Hyperglycemic State
Hypoglycemia and Glucagon
Huntington Disease l: Introduction
Goiter
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Hyperthyroidism I: Introduction
