The intellectual capacity of patients with Laron syndrome (LS) differs with various molecular defects of the growth hormone receptor gene. Correlation with CNS abnormalities

• Published in: Hormone and metabolic research Vol. 37; no. 12; p. 757
• Main Authors: Shevah, O, Kornreich, L, Galatzer, A, Laron, Z
• Format: Journal Article
• Language: English
• Published: Germany 01.12.2005
• Subjects: Adult; Brain - abnormalities; Female; Gene Deletion; Humans; Insulin-Like Growth Factor I - deficiency; Intelligence - genetics; Laron Syndrome - genetics; Magnetic Resonance Imaging; Male; Middle Aged; Point Mutation - genetics; Receptors, Somatotropin - genetics
• ISSN: 0018-5043
• DOI: 10.1055/s-2005-921097

The correlation between the molecular defects of the GH receptor (R), psychosocial development and brain abnormalities were evaluated in 10 patients with Laron syndrome (LS), in whom all data were available. The findings revealed that the intelligence quotient (IQ) and abnormalities in the brain of the patients with LS differ with various molecular defects of the GH-receptor. The most severe mental deficits and brain pathology occurred in patients with 3, 5, 6 exon deletion. Patients with point mutations in exons 2, 4 and 7 presented various degrees of medium to mild CNS abnormalities that correlated with the IQ. Notably, the patient with the E180 splice mutation in exon 6 had a normal IQ, which fits the report on normal IQ in a large Ecuadorian cohort with the same mutation. This is the first report to support a correlation between IQ, brain abnormalities and localization of the molecular defects in the GH-R gene. As all patients with LS are IGF-I-deficient, it must be assumed that other as yet unknown factors related to the molecular defects in the GH-R are the major cause of the differences in intellect and brain abnormalities.