Aniridia ptosis intellectual deficit familial obesity: Difference between revisions
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{{CMG}}'''Assosciate Editor(s)-In-Chief:''' [[User: Prashanthsaddala|Prashanth Saddala M.B.B.S]] | {{CMG}}'''Assosciate Editor(s)-In-Chief:''' [[User: Prashanthsaddala|Prashanth Saddala M.B.B.S]] | ||
{{SK}} | {{SK}} Aniridia - ptosis - mental retardation - obesity familial type complex | ||
Aniridia - ptosis - mental retardation - obesity familial type complex | |||
==Overview== | ==Overview== | ||
The association of ocular abnormalities including partial or complete [[aniridia]], [[ptosis]], pendular [[nystagmus]], corneal [[pannus]], persistent pupillary membrane, lenticular opacities, and foveal hypoplasia was reported only once, in a woman and her two children. All three family members had a visual acuity of 20/200. Several systemic abnormalities also were noted, including [[obesity]] and [[mental retardation]] in the two children, and [[alopecia]], cardiac abnormalities, and frequent spontaneous [[abortion]] in the mother. Family history indicated that the children's maternal grandmother also had similar ocular findings. This constellation of findings probably represents a rare, apparently dominant, variant of aniridia. | The association of ocular abnormalities including partial or complete [[aniridia]], [[ptosis]], pendular [[nystagmus]], corneal [[pannus]], persistent pupillary membrane, lenticular opacities, and foveal hypoplasia was reported only once, in a woman and her two children. All three family members had a visual acuity of 20/200. Several systemic abnormalities also were noted, including [[obesity]] and [[mental retardation]] in the two children, and [[alopecia]], cardiac abnormalities, and frequent spontaneous [[abortion]] in the mother. Family history indicated that the children's maternal grandmother also had similar ocular findings. This constellation of findings probably represents a rare, apparently dominant, variant of aniridia. | ||
==Pathophysiology== | ==Pathophysiology== | ||
===Genetics=== | ===Genetics=== | ||
Autosomal Dominant inheritance | Autosomal Dominant inheritance | ||
==Epidemiology and Demographics== | |||
The prevalence is <1 in 1,000,000. | |||
==References== | ==References== |
Latest revision as of 19:33, 30 July 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Assosciate Editor(s)-In-Chief: Prashanth Saddala M.B.B.S
Synonyms and keywords: Aniridia - ptosis - mental retardation - obesity familial type complex
Overview
The association of ocular abnormalities including partial or complete aniridia, ptosis, pendular nystagmus, corneal pannus, persistent pupillary membrane, lenticular opacities, and foveal hypoplasia was reported only once, in a woman and her two children. All three family members had a visual acuity of 20/200. Several systemic abnormalities also were noted, including obesity and mental retardation in the two children, and alopecia, cardiac abnormalities, and frequent spontaneous abortion in the mother. Family history indicated that the children's maternal grandmother also had similar ocular findings. This constellation of findings probably represents a rare, apparently dominant, variant of aniridia.
Pathophysiology
Genetics
Autosomal Dominant inheritance
Epidemiology and Demographics
The prevalence is <1 in 1,000,000.