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Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome

ORPHA:445062DiseaseAutosomal recessiveAdolescent, Childhood, Infancy

Ассоциированные гены (1)

DNAJC3
DnaJ heat shock protein family (Hsp40) member C3
Disease-causing germline mutation(s) (loss of function) in
OMIM: 601184

Фенотипы (15)

Частый (30–79%)13
HP:0000819Diabetes mellitus
HP:0001272Cerebellar atrophy
HP:0002059Cerebral atrophy
HP:0002066Gait ataxia
HP:0002522Areflexia of lower limbs
HP:0004322Short stature
HP:0004325Decreased body weight
HP:0006827Atrophy of the spinal cord
HP:0007108Demyelinating peripheral neuropathy
HP:0007141Sensorimotor neuropathy
HP:0007366Atrophy/Degeneration affecting the brainstem
HP:0008619Bilateral sensorineural hearing impairment
HP:0010871Sensory ataxia
Периодический (5–29%)2
HP:0001256Intellectual disability, mild
HP:0003487Babinski sign

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы