Hoyeraal-Hreidarsson syndrome

Hoyeraal-Hreidarsson syndrome
[[File:|250px|alt=|]]
Synonyms
Pronounce
Field	N/A
Symptoms	Cerebellar hypoplasia, Immunodeficiency, Bone marrow failure, Microcephaly, Developmental delay
Complications	N/A
Onset
Duration
Types
Causes	Genetic mutation
Risks
Diagnosis	Genetic testing, Clinical evaluation
Differential diagnosis
Prevention
Treatment	Supportive care, Bone marrow transplant
Medication
Prognosis
Frequency
Deaths

Hoyeraal-Hreidarsson syndrome (HHS) is a rare, inherited disorder that is considered a severe variant of dyskeratosis congenita. It is characterized by a combination of cerebellar hypoplasia, immunodeficiency, bone marrow failure, microcephaly, and developmental delay. The syndrome is named after the physicians who first described it.

Presentation

Individuals with Hoyeraal-Hreidarsson syndrome typically present with a range of symptoms that may include:

• Cerebellar hypoplasia: Underdevelopment of the cerebellum, leading to problems with balance and coordination.
• Immunodeficiency: Increased susceptibility to infections due to a weakened immune system.
• Bone marrow failure: Inability of the bone marrow to produce sufficient blood cells, leading to conditions such as anemia, thrombocytopenia, and leukopenia.
• Microcephaly: Abnormally small head size, often associated with intellectual disability.
• Developmental delay: Delays in reaching developmental milestones.

Genetics

Hoyeraal-Hreidarsson syndrome is caused by mutations in genes involved in telomere maintenance. The most commonly affected gene is DKC1, which encodes the protein dyskerin. Mutations in other genes such as RTEL1, TINF2, and POT1 have also been implicated.

Diagnosis

Diagnosis of Hoyeraal-Hreidarsson syndrome is based on clinical evaluation and genetic testing. Key diagnostic features include the presence of cerebellar hypoplasia, immunodeficiency, bone marrow failure, microcephaly, and developmental delay. Genetic testing can confirm mutations in the associated genes.

Treatment

There is no cure for Hoyeraal-Hreidarsson syndrome, and treatment is primarily supportive. Management strategies may include:

• Bone marrow transplant: To address bone marrow failure.
• Immunoglobulin therapy: To boost the immune system.
• Physical therapy: To improve motor skills and coordination.
• Developmental support: Including special education and therapies to support developmental progress.

Prognosis

The prognosis for individuals with Hoyeraal-Hreidarsson syndrome varies depending on the severity of symptoms and the success of treatments such as bone marrow transplant. The condition is often life-threatening due to complications from bone marrow failure and immunodeficiency.

See also

• Dyskeratosis congenita
• Cerebellar hypoplasia
• Immunodeficiency
• Bone marrow failure
• Microcephaly
• Developmental delay

edit 

WikiMD neurology

External links

• Comprehensive information from the National Institute of health.
  

A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z