Pycnodysostosis (PYCD) is an autosomal recessive lysosomal storage disorder of the bone
which leads to stereotypical abnormalities consisting of, but not limited to, sclerotic and …

Background Osteopetrosis is a genetic disease characterized by defects in osteoclast
formation and function. There were a few cases of subtrochanteric femur fractures treated …

Background/Objectives: Pycnodysostosis is a rare genetic disorder causing skeletal
dysplasia. It is determined by a gene mutation leading to cathepsin K deficiency and …

Background: Pycnodysostosis (PYCD) is a rare genetic disorder causing skeletal dysplasia.
It is inherited in an autosomal recessive manner, and it is caused by a gene mutation …

Pycnodysostosis is an autosomal recessive disease caused by a gene mutation leading
cathepsin K deficiency. Pathological fractures of the long bones are common, but guidelines …

Pycnodysostosis is a rare genetic condition that leads to generalised bony sclerosis and
increased fracture risk. Orthopaedic specialists play a crucial role in managing affected …

Pycnodysostosis is a rare inherited disorder of autosomal recessive trait causing cathepsin
K deficiency, leading to failure of osteoclastic activity. Brittle and sclerotic bones which are …

Выполнен анализ данных литературы о применении различных методов
интрамедуллярного остеосинтеза при лечении переломов бедренной кости у детей …

Objetivo: Relatar o caso de picnodisostose em paciente acometido por múltiplas fraturas por
trauma de baixíssima energia. Detalhamento do caso: Paciente de 35 anos, sexo …

Малоинвазивный стабильно-функциональный интрамедуллярный
металлоостеосинтез гибкими титановыми стержнями TEN в последнее десятилетие …