Ultrastructural Sperm Flagellum Defects in a Patient With CCDC39 Compound Heterozygous Mutations and Primary Ciliary Dyskinesia/Situs Viscerum Inversus
Introduction: Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease characterized by structural or functional motile cilia abnormalities. Up to 40 different genes seem, at the moment, to be involved in the pathogenesis of PCD. A number of ultrastructural defects have also been repor...
Main Authors: | Rossella Cannarella, Eugenia Tiziana Maniscalchi, Rosita Angela Condorelli, Marina Scalia, Giulia Guerri, Sandro La Vignera, Matteo Bertelli, Aldo Eugenio Calogero |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2020-08-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fgene.2020.00974/full |
Similar Items
-
Association of bronchectasies and situs inversus
by: H. Kouismi, et al.
Published: (2014-10-01) -
The challenging aspects and successful anaesthetic management in a case of situs inversus totalis
by: Sukhminder Jit Singh Bajwa, et al.
Published: (2012-01-01) -
Kartagener’s Syndrome: Situs Inversus, Chronic Sinusitis and Bronchiectasis
by: Robin Peters, et al.
Published: (2016-02-01) -
LAPAROSCOPIC CHOLECYSTECTOMY IN SITUS INVERSUS TOTALIS VISCERUM
by: N. S. Grigor’ev, et al.
Published: (2016-02-01) -
Situs Inversus Totalis with Hydrocephalus in an Adult: A Rare Case Report
by: Yam Bahadur Roka, et al.
Published: (2019-06-01)