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Trichomegaly-retina pigmentary degeneration-dwarfism syndrome

ORPHA:3363Malformation syndromeAutosomal recessiveInfancy, Neonatal

Ассоциированные гены (1)

PNPLA6
patatin like domain 6, lysophospholipase
Disease-causing germline mutation(s) (loss of function) in
OMIM: 603197

Фенотипы (22)

Очень частый (80–99%)1
HP:0000546Retinal degeneration
Частый (30–79%)14
HP:0000135Hypogonadism
HP:0000527Long eyelashes
HP:0000580Pigmentary retinopathy
HP:0000821Hypothyroidism
HP:0000824Decreased response to growth hormone stimulation test
HP:0001249Intellectual disability
HP:0001251Ataxia
HP:0001510Growth delay
HP:0001518Small for gestational age
HP:0001596Alopecia
HP:0002750Delayed skeletal maturation
HP:0003265Neonatal hyperbilirubinemia
HP:0008070Sparse hair
HP:0009830Peripheral neuropathy
Периодический (5–29%)5
HP:0000028Cryptorchidism
HP:0000054Micropenis
HP:0000164Abnormality of the dentition
HP:0000545Myopia
HP:0002007Frontal bossing
Очень редкий (1–4%)2
HP:0000252Microcephaly
HP:0001250Seizure

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