… do not reliably develop a phenotype similar to pituitary dwarfism. Rather, these patients
exhibit a similar phenotype to that of Laron dwarfism, which was observed in our patient. We …

… Four rare autosomal recessive syndromes associated with a high cancer risk in homozygotes
ataxia telangiectasia (AT), Bloom syndrome (BS), Fanconi anemia (FA), and xeroderma …

… In Reference to Fanconi Anemia and Laron Syndrome … Fanconi Anemia* … Laron Syndrome* …

… of these patients is alive and well, a second patient developed fatal acute myelogenous
leukemia, and the third died of complications after bone marrow transplant for aplastic anemia. …

… study regarding the association of Laron syndrome (LS) and Fanconi anemia (FA); the …
close phenotype to that of the one described by Laron, 1 hence, strongly suggesting a growth …

… receptors, such as Laron dwarfism (growth hormone receptor) … In addition to defining another
disease on the genetic level … disorder that eventuates in aplastic anemia, that can only be …

… a patient with Laron Syndrome and describe the progression to metabolic syndrome, type
2 diabetes, and obesity with a dramatic outcome. Realistic Laron Syndrome prevalence is yet …

… , each in a single family: aplastic anemia, hemochromatosis, infantile polycystic kidneys, … ,
Laron syndrome, and metachromatic leukodystrophy. In several other families a syndrome was …

… receptor gene; therefore, it can be concluded that the fetus will not present with Laron
Syndrome but be a carrier (heterozygote) of Laron syndrome. GHR: Growth hormone receptor. …

… were performed to screen for Fanconi anemia, paroxysmal nocturnal hemoglobinuria, and
myelodysplastic syndrome. Secondary aplastic anemia following toxic exposure, infections, …