Alstrom syndrome

ALMS1 - Alstrom syndrome type 1

This test is available for the following conditions:

• Conditions > Multiple congenital anomalies (MCA) > Alstrom syndrome
• Conditions > Hearing impairment > Alstrom syndrome
• Conditions > Endocrine > Alstrom syndrome
• Conditions > Renal / Nephrological > Alstrom syndrome
• Conditions > Vision impairment / blindness > Alstrom syndrome

This product is also part of the following panels:

• WES ciliopathies (100.0% *)
• WES comprehensive preconception carrier test ¹
• WES hearing impairment (including GJB2) (100.0% *)
• WES heart disorders¹ (100.0% *)
• WES intellectual disability (100.0% *)
• WES intellectual disability (100.0% *)
• WES Mendelian inherited disorders (100.0% *)
• WES Mendelian inherited disorders (100.0% *)
• WES renal disorders (100.0% *)
• WES renal disorders (100.0% *)
• WES short stature/skeletal dysplasia (100.0% *)
• WES vision disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

• Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 606844
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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