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Ring chromosome 1 syndrome

ORPHA:1437Malformation syndromeNeonatal

Фенотипы (13)

Очень частый (80–99%)13
HP:0000252Microcephaly
HP:0000311Round face
HP:0000343Long philtrum
HP:0000431Wide nasal bridge
HP:0000463Anteverted nares
HP:0000494Downslanted palpebral fissures
HP:0000506Telecanthus
HP:0000508Ptosis
HP:0002714Downturned corners of mouth
HP:0004209Clinodactyly of the 5th finger
HP:0008872Feeding difficulties in infancy
HP:0010720Abnormal hair pattern
HP:0100543Cognitive impairment

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