Alport syndrome pathophysiology: Difference between revisions
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==Genetics== | ==Genetics== | ||
Alport syndrome is a rare inherited disease, that is passed down by the mother's or father's X chromosome or a mutation involving chromosome 2. There are three forms of inheritance. It can either be x-linked, autosomal dominant, and autosomal recessive.<ref name="pmid23349312">{{cite journal| author=Savige J, Gregory M, Gross O, Kashtan C, Ding J, Flinter F| title=Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathy. | journal=J Am Soc Nephrol | year= 2013 | volume= 24 | issue= 3 | pages= 364-75 | pmid=23349312 | doi=10.1681/ASN.2012020148 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23349312 }} </ref> | Alport syndrome is a rare inherited disease, that is passed down by the mother's or father's X chromosome or a mutation involving chromosome 2. There are three forms of inheritance. It can either be x-linked, autosomal dominant, and autosomal recessive.<ref name="pmid23349312">{{cite journal| author=Savige J, Gregory M, Gross O, Kashtan C, Ding J, Flinter F| title=Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathy. | journal=J Am Soc Nephrol | year= 2013 | volume= 24 | issue= 3 | pages= 364-75 | pmid=23349312 | doi=10.1681/ASN.2012020148 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23349312 }} </ref> | ||
[[File:Alport Syndrome X-linked Father.jpg]] | [[File:Alport Syndrome X-linked Father.jpg]] | ||
Revision as of 13:40, 2 November 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2]Associate Editor(s)-in-Chief: Krzysztof Wierzbicki M.D. [3]
Overview
Pathogenesis
Genetics
Alport syndrome is a rare inherited disease, that is passed down by the mother's or father's X chromosome or a mutation involving chromosome 2. There are three forms of inheritance. It can either be x-linked, autosomal dominant, and autosomal recessive.[1]
Gross Pathology
Microscopic Pathology
Alport’s syndrome is characterized by the defect of alpha chains of type IV collagen that constitute a triad of manifestations: renal, auditory, and ocular. Involvement of the glomerular basement membrane is the hallmark of Alport’s syndrome.[2][3] It is still controversial as to whether the basement membrane becomes thicker or thinner to induce splitting.
| Manifestations | Renal | Auditory | Ocular |
| Molecular Findings | Absence of collagen network of the glomerular basement membrane (GBM) that is normally formed by podocytes and endothelial cells[4][5][6] | Cellular loss, including hair cells of Corti, and edema associated with atrophy of tissue[7][8][9][10] | Cellular loss and mitochondrial edema. Honeycombing of broken abnormal filaments that are surrounded by vacuolated spheres and membranes[11][8] |
| Histopathological Changes | Lamellated GBM and splitting with appearance of false layers of the basement membrane leading to focal sclerosis of glomeruli[7][8][9][2] | Basement changes of the stria vascularis of the cochlea | Pathological changes involving the lens capsule, the largest basement membrane in the eye[11][8] |
Alpha chains of type IV collagen are located at specific regions in the body. However, the involvement of one type of alpha chain does not necessarily have to involve all corresponding beds that are known to be composed of that same collagen type. To date, there has been no valid hypothesis of why renal, auditory, and ocular manifestations are observed in Alport’s syndrome, but other basement membrane beds involving alpha-5 type IV collagen are no involved, such as the epidermal basement membrane of the skin.[8][12]
References
- ↑ Savige J, Gregory M, Gross O, Kashtan C, Ding J, Flinter F (2013). "Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathy". J Am Soc Nephrol. 24 (3): 364–75. doi:10.1681/ASN.2012020148. PMID 23349312.
- ↑ 2.0 2.1 Bodziak KA, Hammond WS, Molitoris BA (1994). "Inherited diseases of the glomerular basement membrane". Am J Kidney Dis. 23 (4): 605–18. PMID 8154501.
- ↑ Kashtan CE, Michael AF (1993). "Alport syndrome: from bedside to genome to bedside". Am J Kidney Dis. 22 (5): 627–40. PMID 8238007.
- ↑ Abrahamson DR, Hudson BG, Stroganova L, Borza DB, St John PL (2009). "Cellular origins of type IV collagen networks in developing glomeruli". J Am Soc Nephrol. 20 (7): 1471–9. doi:10 .1681/ASN.2008101086 Check
|doi=value (help). PMC 2709682. PMID 19423686. - ↑ Miner JH (1998). "Developmental biology of glomerular basement membrane components". Curr Opin Nephrol Hypertens. 7 (1): 13–9. PMID 9442357.
- ↑ St John PL, Abrahamson DR (2001). "Glomerular endothelial cells and podocytes jointly synthesize laminin-1 and -11 chains". Kidney Int. 60 (3): 1037–46. doi:10.1046/j.1523-1755.2001.0600031037.x. PMID 11532098.
- ↑ 7.0 7.1 Chugh KS, Sakhuja V, Agarwal A, Jha V, Joshi K, Datta BN; et al. (1993). "Hereditary nephritis (Alport's syndrome)--clinical profile and inheritance in 28 kindreds". Nephrol Dial Transplant. 8 (8): 690–5. PMID 8414153.
- ↑ 8.0 8.1 8.2 8.3 8.4 McCarthy PA, Maino DM (2000). "Alport syndrome: a review". Clin Eye Vis Care. 12 (3–4): 139–150. PMID 11137428.
- ↑ 9.0 9.1 Andreoli SP, Deaton M (1992). "Alport's syndrome". Ear Nose Throat J. 71 (10): 508–11. PMID 1425373.
- ↑ Grondalski SJ, Bennett GR (1989). "Alport's syndrome: review and case report". Optom Vis Sci. 66 (6): 396–8. PMID 2771325.
- ↑ 11.0 11.1 Streeten BW, Robinson MR, Wallace R, Jones DB (1987). "Lens capsule abnormalities in Alport's syndrome". Arch Ophthalmol. 105 (12): 1693–7. PMID 3689194.
- ↑ Barker DF, Hostikka SL, Zhou J, Chow LT, Oliphant AR, Gerken SC; et al. (1990). "Identification of mutations in the COL4A5 collagen gene in Alport syndrome". Science. 248 (4960): 1224–7. PMID 2349482.