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Nanophthalmos 2(NNO2)

MedGen UID:
372177
Concept ID:
C1836006
Disease or Syndrome
Synonyms: NANOPHTHALMIA 2; NANOPHTHALMOS, AUTOSOMAL RECESSIVE; NNO2
 
Gene (location): MFRP (11q23.3)
 
Monarch Initiative: MONDO:0012299
OMIM®: 609549

Definition

Any nanophthalmia in which the cause of the disease is a mutation in the MFRP gene. [from MONDO]

Clinical features

From HPO
Microphthalmia
MedGen UID:
10033
Concept ID:
C0026010
Congenital Abnormality
Microphthalmia is an eye abnormality that arises before birth. In this condition, one or both eyeballs are abnormally small. In some affected individuals, the eyeball may appear to be completely missing; however, even in these cases some remaining eye tissue is generally present. Such severe microphthalmia should be distinguished from another condition called anophthalmia, in which no eyeball forms at all. However, the terms anophthalmia and severe microphthalmia are often used interchangeably. Microphthalmia may or may not result in significant vision loss.\n\nPeople with microphthalmia may also have a condition called coloboma. Colobomas are missing pieces of tissue in structures that form the eye. They may appear as notches or gaps in the colored part of the eye called the iris; the retina, which is the specialized light-sensitive tissue that lines the back of the eye; the blood vessel layer under the retina called the choroid; or in the optic nerves, which carry information from the eyes to the brain. Colobomas may be present in one or both eyes and, depending on their size and location, can affect a person's vision.\n\nPeople with microphthalmia may also have other eye abnormalities, including clouding of the lens of the eye (cataract) and a narrowed opening of the eye (narrowed palpebral fissure). Additionally, affected individuals may have an abnormality called microcornea, in which the clear front covering of the eye (cornea) is small and abnormally curved.\n\nBetween one-third and one-half of affected individuals have microphthalmia as part of a syndrome that affects other organs and tissues in the body. These forms of the condition are described as syndromic. When microphthalmia occurs by itself, it is described as nonsyndromic or isolated.

Recent clinical studies

Etiology

Almoallem B, Arno G, De Zaeytijd J, Verdin H, Balikova I, Casteels I, de Ravel T, Hull S, Suzani M, Destrée A, Peng M, Williams D, Ainsworth JR, Webster AR, Leroy BP, Moore AT, De Baere E
Sci Rep 2020 Jan 28;10(1):1289. doi: 10.1038/s41598-019-57338-2. PMID: 31992737Free PMC Article

Diagnosis

Almoallem B, Arno G, De Zaeytijd J, Verdin H, Balikova I, Casteels I, de Ravel T, Hull S, Suzani M, Destrée A, Peng M, Williams D, Ainsworth JR, Webster AR, Leroy BP, Moore AT, De Baere E
Sci Rep 2020 Jan 28;10(1):1289. doi: 10.1038/s41598-019-57338-2. PMID: 31992737Free PMC Article

Clinical prediction guides

Almoallem B, Arno G, De Zaeytijd J, Verdin H, Balikova I, Casteels I, de Ravel T, Hull S, Suzani M, Destrée A, Peng M, Williams D, Ainsworth JR, Webster AR, Leroy BP, Moore AT, De Baere E
Sci Rep 2020 Jan 28;10(1):1289. doi: 10.1038/s41598-019-57338-2. PMID: 31992737Free PMC Article

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