0000000001134416

AUTHOR

Helen Puusepp

showing 1 related works from this author

Girl With Partial Turner Syndrome and Absence Epilepsy

2007

This report describes a 16-year-old girl with short stature (-5 standard deviations), normal puberty, panic attacks, absence epilepsy, some stigmata of Turner syndrome, and a Madelung deformity. Routine chromosomal analysis revealed a female karyotype with one abnormal chromosome X, with the suspicion of additional material on the short arm. With fluorescent in situ hybridization and array-multiplex amplifiable probe hybridization methodology, a complex aberration was detected, with a deletion of the distal part of Xp22.33 (including the short-stature homeobox gene) and a duplication of Xp22.32-p22.12 proximal to the deleted segment. The deletion in our patient involves the Xp22.33 region. …

Homeodomain ProteinsGeneticsAdolescentTurner SyndromeKaryotypeBiologymedicine.diseaseShort statureEpilepsy AbsenceShort Stature Homeobox ProteinDevelopmental NeuroscienceNeurologyShort Stature Homeobox ProteinPediatrics Perinatology and Child HealthGene duplicationTurner syndromemedicineOMIM : Online Mendelian Inheritance in ManHumansHomeoboxFemaleNeurology (clinical)medicine.symptomX chromosomePediatric Neurology
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