Ayazi syndrome

Ayazi syndrome (tàbí Chromosome 21 Xq21 deletion syndrome)^[1] àmìn àrùn tí a maa ń rí bí ènìyàn bá ní àrùn choroideremia, ìdití abínibí àti ìsanrajù.

Àmin ìdánilójú àtúnṣe

Àìpé ọpọlọ
ìdití latinú oyún
Ìsanrajù
Choroideremia
àìrí ìràn dáradára
Àrun ojú

Ìmọ̀ nípa abínibírẹ̀ àtúnṣe

Wọ́n ṣàpèjúwe bí ìbíni mọ́ Ayazi syndrome jẹ́ x-linked recessive. CHM àti POU3F4, ni àwọn gíìnì tó sọnù ní ipò Xq21 locus tí wọ́n wà.^[1]

Àwọn ìtọ́kasí àtúnṣe

↑ ^1.0 ^1.1 "OMIM Entry - # 303110 - CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION". www.omim.org.

Ayazi S (1981). "Choroideremia, obesity, and congenital deafness". Am J Ophthalmol 92 (1): 63–69. PMID 7258279.
"Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21". Am J Hum Genet 45 (4): 530–540. 1989. PMC 1683514. PMID 2491012. //www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1683514.
http://www.wrongdiagnosis.com/a/ayazi_syndrome/symptoms.htm

Àwọn ìjápọ̀ látìta àtúnṣe

Online 'Mendelian Inheritance in Man' (OMIM) 303110

[:0-1] 1.0 ^1.1 "OMIM Entry - # 303110 - CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION". www.omim.org.

[1]