This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.
|Medical Terms||Other Names||
|30%-79% of people have these symptoms|
|Abnormal sperm motility||0012206|
|Chronic otitis media||
Chronic infections of the middle ear
Blockage of nose
Obstruction of nose
Stuffy nose[ more ]
|Neonatal respiratory distress||
Infantile respiratory distress
Newborn respiratory distress
Respiratory distress, neonatal[ more ]
|Recurrent otitis media||
Recurrent middle ear infection
|Recurrent sinopulmonary infections||
Recurrent sinus and lung infections
|5%-29% of people have these symptoms|
Partial or complete collapse of part or entire lung
Permanent enlargement of the airways of the lungs
Clubbing of fingers and toes
|Conductive hearing impairment||
Conductive hearing loss[ more ]
|Delayed speech and language development||
Deficiency of speech development
Delayed language development
Delayed speech acquisition
Delayed speech development
Impaired speech and language development
Impaired speech development
Language development deficit
Late-onset speech development
Poor language development
Speech and language delay
Speech and language difficulties
Speech delay[ more ]
|Peribronchovascular interstitial thickening||0025177|
Obstructive lung disease
|Pulmonary situs ambiguus||0011617|
|Recurrent mycobacterial infections||0011274|
|Situs inversus totalis||
All organs on wrong side of body
|1%-4% of people have these symptoms|
|Abnormal inferior vena cava morphology||0025576|
|Anomalous pulmonary venous return||0010772|
|Atrial situs ambiguous||0011539|
|Double outlet right ventricle||0001719|
Too much cerebrospinal fluid in the brain
|Persistent left superior vena cava||0005301|
Multiple small spleens
|Transposition of the great arteries||0001669|
Making a diagnosis for a genetic or rare disease can often be challenging. Healthcare professionals typically look at a person’s medical history, symptoms, physical exam, and laboratory test results in order to make a diagnosis. The following resources provide information relating to diagnosis and testing for this condition. If you have questions about getting a diagnosis, you should contact a healthcare professional.
Related diseases are conditions that have similar signs and symptoms. A health care provider may consider these conditions in the table below when making a diagnosis. Please note that the table may not include all the possible conditions related to this disease.
Conditions with similar signs and symptoms from Orphanet
The main differential diagnoses are cystic fibrosis, immunodeficiency syndromes and gastroesophageal reflux. Additionally, PCD has been noted in patients with Cri du chat syndrome due to the common locus on chromosome 5p. Segmental deletion of chromosome 5p in Cri du chat syndrome usually includes PCD-associated gene DNAH5 and the pathogenic variant in the remaining allele of DNAH5 renders it to PCD.
Visit the Orphanet disease page for more information.
Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
Questions sent to GARD may be posted here if the information could be helpful to others. We remove all identifying information when posting a question to protect your privacy. If you do not want your question posted, please let us know. Submit a new question
Can you please provide me with some doctors that specialize in primary ciliary dyskinesia or that have knowledge treating this disorder? See answer
Is there a support group for people with primary ciliary dyskinesia? How many people have been diagnosed with primary ciliary dyskinesia? What is their work status? See answer