Pediatric facial erythema dwarf syndrome

Facial telangiectasis of dwarfs syndrome is an autosomal recessive hereditary disease, which is mainly manifested by three major clinical features such as dwarf, light-sensitive and facial telangiectasia. Bloom first reported congenital capillary dilatation erythema dwarf called lupus erythematosus. In 1983, a case was reported by Zeng's disease in China, which was called domestic erythema dwarf syndrome, dwarf facial telangiectasia, intrauterine dwarf sign, primordial dwarf, congenital telangiectasia and so on. This symptom is also known as congenital telangiectastic erythema, Bloom syndrome, chromosome instability syndrome, dwarf capillary vasodilation, chromosomal fragility syndrome, chromosomes Rupture syndrome (chromosomal leakage Bloom-Torre-Mackacek syndrome).