Differentiating Albinism from other diseases: Difference between revisions

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Latest revision as of 23:21, 23 August 2021

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shadan Mehraban, M.D.[2]

Overview

Oculocutaneous albinism and ocular albinism must be differentiated from the following rare disease: Hermansky-Pudlak syndrome, Chediak-Higashi syndrome, Griscelli syndrome, Waardenburg syndrome type II, Vici syndrome, Tietz albinism-deafness syndrome, Angelman syndrome, Prader-Willi syndrome, Cross-McKusick-Breen syndrome, Achromatopsia, Aland Island eye disease (Forsius-Eriksson syndrome), Aniridia, and Congenital nystagmus.

Differential Diagnosis

Oculocutaneous albinism and ocular albinism must be differentiated from following disorders:^[1]^[2]^[3]^[4]^[5]^[6]^[7]^[8]^[9]

Differential diagnosis of Albinism
Disease	Inheritance	Gene mutation	Diagnostic criteria
Hermansky-Pudlak syndrome	Autosomal recessive	Affected genes of lysosome-related organelles	Oculocutaneous albinism Accumulation of ceroid in tissues Immunologic deficiency Interstitial lung fibrosis Granulomatous colitis Bleeding problem (deficiency of granules in platelets)
Chediak-Higashi syndrome	Autosomal recessive	Lysosomal trafficking regulator gene	Oculocutaneous albinism Increased susceptibility to bacterial infection Increased bleeding time Peripheral neuropathy
Griscelli syndrome	Autosomal recessive	Defects in myosin, myosin receptors, and binding	Albinism Immune impairment Neurological deficit Melanin aggregation in hair shaft
Waardenburg syndrome type II	Autosomal dominant	MITF gene mutation	Patchy skin hypopigmentation Iris heterochromia sensorineural hearing loss
Vici syndrome	Autosomal recessive	Mutation in ectopic P granules protein 5	Absent of corpus callosum Skin and hair hypopigmentation Microcephaly Immunodeficiency Cardiac abnormalities Cataracts Cleft lip and palate Neurologic abnormalities
Tietz albinism-deafness syndrome	Autosomal dominant	MITF gene mutation	White eyebrows and eyelashes Iris hypopigmentation Sensorineural hearing loss
Angelman syndrome	Loss of the maternal copy of chromosome 15q11.2-13	-	Skin and hair hypopigmentation characteristic facial features Short stature Mental retardation Spastic gait Seizure Inappropriate outburst of laughter
Prader-Willi syndrome	Loss of the paternal copy of chromosome 15q11.2-13	-	Skin and hair hypopigmentation Poor muscle tone Short stature Mental retardation Hyperphagia leads obesity and type 2 diabetes
Cross-McKusick-Breen syndrome	Autosomal recessive	De novo interstitial deletion of (3)(q27.1q29) of the paternal chromosome	Skin and hair hypopigmentation Microphthalmia Corneal opacification Nystagmus Athetosis Ataxia Joint contractures Spastic tetraplegia
Achromatopsia	Autosomal recessive	Dysfunctional cone cells in the retina	Loss of color vision Photophobia Nystagmus Low visual acuity with hyperopia
Aland Island eye disease (Forsius-Eriksson syndrome)	X-linked recessive	Novel CACNA1F gene mutation	fundal hypopigmentation Foveal hypoplasia Myopia and astigmatism Nystagmus Night blindness
Aniridia	Autosomal dominant	PAX6 gene mutation	Absence of the iris Foveal hypoplasia nystagmus Amblyopia cataracts
Congenital nystagmus	X-linked disorder	FRMD7 gene mutation	Nystagmus Reduced visual acuity

References

↑ "Albinism - StatPearls - NCBI Bookshelf".
↑ Lee ST, Nicholls RD, Bundey S, Laxova R, Musarella M, Spritz RA (1994). "Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism". N Engl J Med. 330 (8): 529–34. doi:10.1056/NEJM199402243300803. PMID 8302318.
↑ HERMANSKY F, PUDLAK P (1959). "Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies". Blood. 14 (2): 162–9. PMID 13618373.
↑ DePinho RA, Kaplan KL (1985). "The Hermansky-Pudlak syndrome. Report of three cases and review of pathophysiology and management considerations". Medicine (Baltimore). 64 (3): 192–202. PMID 3921802.
↑ Witkop CJ, Nuñez Babcock M, Rao GH, Gaudier F, Summers CG, Shanahan F; et al. (1990). "Albinism and Hermansky-Pudlak syndrome in Puerto Rico". Bol Asoc Med P R. 82 (8): 333–9. PMID 2261023.
↑ Dimson O, Drolet BA, Esterly NB (1999). "Hermansky-Pudlak syndrome". Pediatr Dermatol. 16 (6): 475–7. doi:10.1046/j.1525-1470.1999.00122.x. PMID 10632950.
↑ Fukai K, Ishii M, Kadoya A, Chanoki M, Hamada T (1993). "Chédiak-Higashi syndrome: report of a case and review of the Japanese literature". J Dermatol. 20 (4): 231–7. doi:10.1111/j.1346-8138.1993.tb03867.x. PMID 8315113.
↑ Mancini AJ, Chan LS, Paller AS (1998). "Partial albinism with immunodeficiency: Griscelli syndrome: report of a case and review of the literature". J Am Acad Dermatol. 38 (2 Pt 2): 295–300. doi:10.1016/s0190-9622(98)70568-7. PMID 9486701.
↑ WAARDENBURG PJ (1951). "A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness". Am J Hum Genet. 3 (3): 195–253. PMC 1716407. PMID 14902764.

Template:WS Template:WH

[1] "Albinism - StatPearls - NCBI Bookshelf".

[pmid8302318-2] Lee ST, Nicholls RD, Bundey S, Laxova R, Musarella M, Spritz RA (1994). "Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism". N Engl J Med. 330 (8): 529–34. doi:10.1056/NEJM199402243300803. PMID 8302318.

[pmid13618373-3] HERMANSKY F, PUDLAK P (1959). "Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies". Blood. 14 (2): 162–9. PMID 13618373.

[pmid3921802-4] DePinho RA, Kaplan KL (1985). "The Hermansky-Pudlak syndrome. Report of three cases and review of pathophysiology and management considerations". Medicine (Baltimore). 64 (3): 192–202. PMID 3921802.

[pmid2261023-5] Witkop CJ, Nuñez Babcock M, Rao GH, Gaudier F, Summers CG, Shanahan F; et al. (1990). "Albinism and Hermansky-Pudlak syndrome in Puerto Rico". Bol Asoc Med P R. 82 (8): 333–9. PMID 2261023.

[pmid10632950-6] Dimson O, Drolet BA, Esterly NB (1999). "Hermansky-Pudlak syndrome". Pediatr Dermatol. 16 (6): 475–7. doi:10.1046/j.1525-1470.1999.00122.x. PMID 10632950.

[pmid8315113-7] Fukai K, Ishii M, Kadoya A, Chanoki M, Hamada T (1993). "Chédiak-Higashi syndrome: report of a case and review of the Japanese literature". J Dermatol. 20 (4): 231–7. doi:10.1111/j.1346-8138.1993.tb03867.x. PMID 8315113.

[pmid9486701-8] Mancini AJ, Chan LS, Paller AS (1998). "Partial albinism with immunodeficiency: Griscelli syndrome: report of a case and review of the literature". J Am Acad Dermatol. 38 (2 Pt 2): 295–300. doi:10.1016/s0190-9622(98)70568-7. PMID 9486701.

[pmid14902764-9] WAARDENBURG PJ (1951). "A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness". Am J Hum Genet. 3 (3): 195–253. PMC 1716407. PMID 14902764.

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@@ Line 4: / Line 4: @@
 ==Overview==
-* Oculocutaneous albinism and ocular albinism must be differentiated from the following rare disease: [[Hermansky-Pudlak syndrome]], [[Chediak-Higashi syndrome]], [[Griscelli syndrome]], [[Waardenburg syndrome]] type II, [[Vici syndrome]], Tietz albinism-deafness syndrome, [[Angelman syndrome]], [[Prader-Willi syndrome]], [[Cross-McKusick-Breen syndrome]], [[Achromatopsia]], Aland Island eye disease (Forsius-Eriksson syndrome), [[Aniridia]], and [[Congenital]] [[nystagmus]].
+[[Oculocutaneous albinism]] and [[ocular albinism]] must be differentiated from the following rare disease: [[Hermansky-Pudlak syndrome]], [[Chediak-Higashi syndrome]], [[Griscelli syndrome]], [[Waardenburg syndrome]] type II, [[Vici syndrome]], Tietz albinism-deafness syndrome, [[Angelman syndrome]], [[Prader-Willi syndrome]], Cross-McKusick-Breen syndrome, [[Achromatopsia]], Aland Island eye disease (Forsius-Eriksson syndrome), [[Aniridia]], and [[Congenital]] [[nystagmus]].
 ==Differential Diagnosis==
 * [[Oculocutaneous albinism]] and [[ocular albinism]] must be differentiated from following disorders:<ref>{{cite web |url=https://www.ncbi.nlm.nih.gov/books/NBK519018/ |title=Albinism - StatPearls - NCBI Bookshelf |format= |work= |accessdate=}}</ref><ref name="pmid8302318">{{cite journal| author=Lee ST, Nicholls RD, Bundey S, Laxova R, Musarella M, Spritz RA| title=Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism. | journal=N Engl J Med | year= 1994 | volume= 330 | issue= 8 | pages= 529-34 | pmid=8302318 | doi=10.1056/NEJM199402243300803 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8302318  }} </ref><ref name="pmid13618373">{{cite journal| author=HERMANSKY F, PUDLAK P| title=Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies. | journal=Blood | year= 1959 | volume= 14 | issue= 2 | pages= 162-9 | pmid=13618373 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=13618373  }} </ref><ref name="pmid3921802">{{cite journal| author=DePinho RA, Kaplan KL| title=The Hermansky-Pudlak syndrome. Report of three cases and review of pathophysiology and management considerations. | journal=Medicine (Baltimore) | year= 1985 | volume= 64 | issue= 3 | pages= 192-202 | pmid=3921802 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3921802  }} </ref><ref name="pmid2261023">{{cite journal| author=Witkop CJ, Nuñez Babcock M, Rao GH, Gaudier F, Summers CG, Shanahan F | display-authors=etal| title=Albinism and Hermansky-Pudlak syndrome in Puerto Rico. | journal=Bol Asoc Med P R | year= 1990 | volume= 82 | issue= 8 | pages= 333-9 | pmid=2261023 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2261023  }} </ref><ref name="pmid10632950">{{cite journal| author=Dimson O, Drolet BA, Esterly NB| title=Hermansky-Pudlak syndrome. | journal=Pediatr Dermatol | year= 1999 | volume= 16 | issue= 6 | pages= 475-7 | pmid=10632950 | doi=10.1046/j.1525-1470.1999.00122.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10632950  }} </ref><ref name="pmid8315113">{{cite journal| author=Fukai K, Ishii M, Kadoya A, Chanoki M, Hamada T| title=Chédiak-Higashi syndrome: report of a case and review of the Japanese literature. | journal=J Dermatol | year= 1993 | volume= 20 | issue= 4 | pages= 231-7 | pmid=8315113 | doi=10.1111/j.1346-8138.1993.tb03867.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8315113  }} </ref><ref name="pmid9486701">{{cite journal| author=Mancini AJ, Chan LS, Paller AS| title=Partial albinism with immunodeficiency: Griscelli syndrome: report of a case and review of the literature. | journal=J Am Acad Dermatol | year= 1998 | volume= 38 | issue= 2 Pt 2 | pages= 295-300 | pmid=9486701 | doi=10.1016/s0190-9622(98)70568-7 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9486701  }} </ref><ref name="pmid14902764">{{cite journal| author=WAARDENBURG PJ| title=A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness. | journal=Am J Hum Genet | year= 1951 | volume= 3 | issue= 3 | pages= 195-253 | pmid=14902764 | doi= | pmc=1716407 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14902764  }} </ref>
@@ Line 120: / Line 121: @@
 | style="background:#DCDCDC;" align="center" + | Aland Island eye disease (Forsius-Eriksson syndrome)
 | style="background:#F5F5F5;" + | [[X-linked recessive]]
-| style="background:#F5F5F5;" + | Novel CACNA1F gene mutation
+| style="background:#F5F5F5;" + | Novel [[CACNA1F]] [[gene mutation]]
 | style="background:#F5F5F5;" + |
 * fundal [[hypopigmentation]]
@@ Line 140: / Line 141: @@
 | style="background:#DCDCDC;" align="center" + | [[Congenital]] [[nystagmus]]
 | style="background:#F5F5F5;" + | [[X-linked]] disorder
-| style="background:#F5F5F5;" + | FRMD7 gene mutation
+| style="background:#F5F5F5;" + | [[FRMD7]] [[gene mutation]]
 | style="background:#F5F5F5;" + |
 * [[Nystagmus]]

Differentiating Albinism from other diseases: Difference between revisions

Latest revision as of 23:21, 23 August 2021

Overview

Differential Diagnosis

References

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