H syndrome

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
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W8MD medical weight loss NYC and sleep center NYC

H syndrome
Synonyms	Histiocytosis-lymphadenopathy plus syndrome
Pronounce	N/A
Specialty	N/A
Symptoms	Hyperpigmentation, hypertrichosis, hepatosplenomegaly, hearing loss, heart anomalies, hypogonadism, short stature, insulin-dependent diabetes mellitus
Complications	N/A
Onset	Childhood
Duration	Lifelong
Types	N/A
Causes	Mutations in the SLC29A3 gene
Risks	Family history of the condition
Diagnosis	Genetic testing, clinical evaluation
Differential diagnosis	Langerhans cell histiocytosis, Rosai-Dorfman disease, Faisalabad histiocytosis
Prevention	N/A
Treatment	Symptomatic management
Medication	N/A
Prognosis	Variable, depending on the severity of symptoms
Frequency	Rare
Deaths	N/A

H syndrome is a rare, autosomal recessive genetic disorder characterized by a constellation of clinical features. The syndrome was first described in the medical literature in 2008, and it is caused by mutations in the SLC29A3 gene, which encodes the human equilibrative nucleoside transporter 3 (hENT3). This transporter is involved in the uptake of nucleosides, which are important for DNA repair and replication, from the extracellular space into cells. The exact mechanism by which mutations in the SLC29A3 gene lead to the diverse symptoms of H syndrome is not fully understood, but it is thought to involve disturbances in nucleoside metabolism and signaling pathways.

Symptoms

H syndrome presents with a wide range of clinical manifestations, which can vary significantly among affected individuals. Common symptoms include:

• Hyperpigmentation and hypertrichosis, particularly on the inner thighs and other areas of the body.
• Hepatomegaly (enlarged liver) or hepatosplenomegaly (enlarged liver and spleen).
• Sensorineural hearing loss.
• Short stature.
• Insulin-dependent diabetes mellitus.
• Lymphadenopathy (swelling of the lymph nodes).
• Cardiomyopathy (disease of the heart muscle).
• Skeletal abnormalities, such as joint contractures and hallux valgus (deformity of the big toe).

Diagnosis

Diagnosis of H syndrome is based on the clinical presentation and confirmed by genetic testing showing mutations in the SLC29A3 gene. Due to the rarity of the condition and the diversity of its symptoms, H syndrome can be difficult to diagnose. A multidisciplinary approach involving pediatricians, endocrinologists, dermatologists, and geneticists is often necessary to accurately diagnose and manage the condition.

Treatment

There is no cure for H syndrome, and treatment is symptomatic and supportive. Management strategies may include:

• Control of diabetes with insulin and dietary modifications.
• Hearing aids for sensorineural hearing loss.
• Physical therapy to manage joint contractures and improve mobility.
• Regular monitoring and treatment for cardiac and liver involvement.

Epidemiology

H syndrome is extremely rare, with only a few dozen cases reported in the medical literature worldwide. It affects males and females equally and has been described in individuals of various ethnic backgrounds.

Research Directions

Research on H syndrome is focused on understanding the precise role of the SLC29A3 gene in the disease, developing targeted therapies, and improving diagnostic methods. Gene therapy and other advanced treatments may offer hope for affected individuals in the future.

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