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Interdisciplinary CompetenceMolecular Diagnostics
Know how in the analysis of genetic material.
For the benefit of patients.

IllnessTeratozoospermie, Differentialdiagnose

Summary

Short information

TP4040_KI

ID
TP4040
Number of loci
Loci typeCount
Gen13
Accredited laboratory test
Examined sequence length
4,0 kb (Core-/Core-canditate-Genes)
35,8 kb (Extended panel: incl. additional genes)
Analysis Duration
on request
Test material
  • EDTA-anticoagulated blood (3-5 ml)
Diagnostic indications

Sanger +

 

Loci panel

Gen

NameExon Length (bp)OMIM-GReferenz-Seq.Heredity
AURKC930NM_001015878.2AR
DPY19L22277NM_173812.5AR
SYCP3711NM_153694.5AD
BRDT2874NM_001242805.2AR
CCDC622055NM_201435.5AR
CEP1123295NM_001199165.4AR
DNAH612648NM_001370.2AR
PICK11248NM_012407.4AR
PMFBP13170NM_031293.3AR
SPATA161710NM_031955.6AR
SUN51397NM_080675.4AR
TSGA102370NM_025244.4AR
ZPBP1056NM_007009.3AR

Informations about the disease

Clinical Comment

Male infertility due to teratozoospermia due to a single gene mutation is a rare genetic cause of male infertility due to altered morphology, such as macrozoospermia or globozoospermia, in over 85% of the sperm. Some genes in mutated form are known to cause teratozoospermia. This is a heterogeneous group of disorders encompassing a broad spectrum of abnormal sperm phenotypes affecting exclusively or simultaneously the head, neck, midpiece, and/or tail. Head integrity is critical for normal sperm function, and head defects consistently result in male infertility. The DNA-diagnostic yield is unknown. An inconspicuous molecular genetic result does not exclude the clinical diagnosis

Reference: doi: 10.1016/j.beem.2020.101473.

 

Synonyms
  • Allelic: Pregnancy loss, recurrent, 4 (SYCP3)
  • "Globozoospermia" (CCDC62)
  • "Macrozoospermia" (AURKC)
  • "Teratozoospermia" (PICK1)
  • "Teratozoospermia" (ZPBP)
  • Heterotaxy; male infertility [panelapp] (DNAH6)
  • Spermatogenic failure 16 (SUN5)
  • Spermatogenic failure 21 (BRDT)
  • Spermatogenic failure 26 (TSGA10)
  • Spermatogenic failure 31 (PMFBP1)
  • Spermatogenic failure 4 (SYCP3)
  • Spermatogenic failure 44 (CEP112)
  • Spermatogenic failure 5 (AURKC)
  • Spermatogenic failure 6 (SPATA16)
  • Spermatogenic failure 9 (DPY19L2)
Heredity, heredity patterns etc.
  • AD
  • AR
OMIM-Ps
  • Multiple OMIM-Ps
ICD10 Code

Bioinformatics and clinical interpretation

No text defined