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Proteus-like syndrome

ORPHA:2969Clinical subtypeAutosomal dominantInfancy, Neonatal

Ассоциированные гены (1)

PTEN
phosphatase and tensin homolog
Disease-causing germline mutation(s) in
OMIM: 601728

Фенотипы (31)

Очень частый (80–99%)12
HP:0000545Myopia
HP:0000615Abnormal pupil morphology
HP:0001028Hemangioma
HP:0001031Subcutaneous lipoma
HP:0001140Limbal dermoid
HP:0001249Intellectual disability
HP:0002816Genu recurvatum
HP:0007400Irregular hyperpigmentation
HP:0010807Open bite
HP:0010816Epidermal nevus
HP:0100559Lower limb asymmetry
HP:0100774Hyperostosis
Частый (30–79%)11
HP:0000238Hydrocephalus
HP:0000256Macrocephaly
HP:0000303Mandibular prognathia
HP:0000518Cataract
HP:0000541Retinal detachment
HP:0000828Abnormality of the parathyroid gland
HP:0001100Heterochromia iridis
HP:0001334Communicating hydrocephalus
HP:0005293Venous insufficiency
HP:0009721Shagreen patch
HP:0100777Exostoses
Периодический (5–29%)8
HP:0000147Polycystic ovaries
HP:0000268Dolichocephaly
HP:0000463Anteverted nares
HP:0000494Downslanted palpebral fissures
HP:0001744Splenomegaly
HP:0002652Skeletal dysplasia
HP:0010516Thymus hyperplasia
HP:0100730Bronchogenic cyst

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы