Linear skin defects with multiple congenital anomalies 2

MONDO:0010474

Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the COX7B gene.

Also known as: COX7B microphthalmia with linear skin defects syndrome, linear skin defects with multiple congenital anomalies 2, linear skin defects with multiple congenital anomalies 2, X-linked dominant, linear skin defects with multiple congenital anomalies type 2, microphthalmia with linear skin defects syndrome caused by mutation in COX7B, LSDMCA2, aplasia cutis congenita, Reticulolinear, with microcephaly, Facial Dysmorphism, and Other congenital anomalies

16 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Eye disorder (97) Syndromic disease (24) Human disease (14) Hereditary skin disorder (5) Microphthalmia (5) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2)

Trials to join now! 11 Not yet recruiting 1 Not yet finished but already full! 2 Completed 1 Terminated 1

VR headsets tested as a possible treatment for blindness

Disease control Terminated

This study tested whether using a virtual reality headset for one-hour sessions could help regenerate damaged optic nerves and improve vision in people with glaucoma or other retinal diseases. The idea came from promising results in rodents. However, the trial was terminated earl…

Phase: NA • Sponsor: Stanford University • Aim: Disease control

Last updated Jun 27, 2026 08:03 UTC

Linear skin defects with multiple congenital anomalies 2

Broader categories

VR headsets tested as a possible treatment for blindness