Malignant infantile osteopetrosis

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Malignant infantile osteopetrosis
Synonyms	Albers-Schönberg disease, marble bone disease
Pronounce	N/A
Specialty	Hematology, Orthopedics
Symptoms	Bone pain, Fractures, Anemia, Hepatosplenomegaly, Blindness, Deafness
Complications	Bone marrow failure, Infections, Neurological deficits
Onset	Infancy
Duration	Lifelong
Types	N/A
Causes	Genetic mutation
Risks	Family history
Diagnosis	X-ray, Genetic testing
Differential diagnosis	Osteoporosis, Rickets, Paget's disease of bone
Prevention	N/A
Treatment	Hematopoietic stem cell transplantation, Interferon gamma-1b, Vitamin D
Medication	N/A
Prognosis	Poor without treatment
Frequency	Rare
Deaths	N/A

Malignant Infantile Osteopetrosis (MIOP), also known as infantile malignant osteopetrosis, is a rare, severe bone disorder that manifests early in infancy. It is characterized by the excessive formation and density of bone, which leads to a variety of complications. This condition is a form of osteopetrosis, a group of disorders affecting bone growth and density. MIOP is considered the most severe form of osteopetrosis and is inherited in an autosomal recessive manner.

Etiology and Pathogenesis

Malignant Infantile Osteopetrosis is caused by mutations in several genes, including TCIRG1, CLCN7, and OSTM1, which are crucial for the normal function of osteoclasts. Osteoclasts are cells responsible for bone resorption, a process essential for the maintenance of healthy bone tissue. Mutations in these genes lead to dysfunctional osteoclasts, resulting in the abnormal accumulation of bone and the hallmark feature of osteopetrosis: increased bone density.

Clinical Features

The clinical manifestations of MIOP are diverse and can include:

• Failure to thrive
• Hepatosplenomegaly (enlargement of the liver and spleen)
• Cranial nerve deficits leading to vision and hearing loss
• Hydrocephalus (accumulation of cerebrospinal fluid in the brain)
• Frequent bone fractures
• Anemia and other hematologic abnormalities due to bone marrow failure

Diagnosis

Diagnosis of Malignant Infantile Osteopetrosis is based on clinical presentation, radiographic findings, and genetic testing. Radiographs typically show generalized increased bone density, particularly at the skull base and long bones. Genetic testing can confirm the diagnosis by identifying mutations in the genes associated with the condition.

Treatment

Treatment options for MIOP are limited and focus on managing symptoms and complications. Current therapies include:

• Bone marrow transplantation (BMT), which can cure the bone marrow failure and correct some of the skeletal abnormalities
• Interferon gamma-1b therapy, which has been shown to improve white blood cell function and increase bone resorption
• Supportive care for complications such as anemia, fractures, and cranial nerve deficits

Prognosis

The prognosis for untreated Malignant Infantile Osteopetrosis is poor, with most affected children not surviving past early childhood due to complications such as bone marrow failure and infections. However, successful bone marrow transplantation can significantly improve life expectancy and quality of life.

Epidemiology

Malignant Infantile Osteopetrosis is a rare disorder, with an estimated incidence of 1 in 250,000 to 300,000 live births worldwide. It affects males and females equally.

See Also

• Osteoclast
• Bone marrow transplantation
• Genetic testing

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