Vertrouwensscore 8/100
Dr Mohammad Al-Shinnag
Clinical Genetics · Darlinghurst
👤 16 jaar ervaring
10,952+
Patients seen
16
Years in practice
4
Publications
1
Languages spoken
Over
Dr. Mohmmad Al-Shinnag is a skilled clinical geneticist specialising in developmental delay, intellectual disability, and neurodevelopmental disorders. With a commitment to understanding the genetic factors underlying these conditions, he employs advanced genetic testing methods, including whole exome sequencing and whole genome sequencing, to investigate and diagnose children facing developmental delay, intellectual disability, and complex health issues.
His comprehensive services include clinical assessment for identifying underlying genetic conditions and providing clinical and molecular diagnoses for affected children. Dr. Al-Shinnag also plays a crucial role in genetic counselling, offering valuable advice on the risk of genetic conditions recurring within families. He assists individuals and couples in reproductive planning, providing insights and guidance for future pregnancies based on their genetic profiles. Moreover, he offers expert guidance on managing these conditions once a diagnosis is established.
Dr. Al-Shinnag holds prestigious fellowships with the Royal Australasian College of Physicians and the Human Genetics Society of Australasia. He serves as a staff specialist at the clinical genomics unit at St Vincent's Hospital Sydney. He completed physician training at the Royal Brisbane and Women's Hospital (RBWH) and advanced training in clinical genetics at Genetic Health Queensland across various hospitals.
The diagnostic genetics services offered by Dr. Al-Shinnag and his team include clinical assessments, investigation reviews, and genetic testing aimed at establishing accurate diagnoses. These diagnoses are instrumental in managing the conditions effectively and providing information to at-risk family members and those planning to expand their families.
Dr. Al-Shinnag's service specialises in addressing a range of conditions, some of which include congenital anomalies, intellectual disability, developmental delay, dysmorphic features, cardiac malformations and diseases, hearing loss, neurological and muscular disorders (such as genetic epilepsy, hereditary spastic paraparesis, peripheral neuropathy, and muscular dystrophy), and eye disorders (including retinitis pigmentosa, congenital cataract, early or late onset macular dystrophy, and various other retinal diseases).
His comprehensive services include clinical assessment for identifying underlying genetic conditions and providing clinical and molecular diagnoses for affected children. Dr. Al-Shinnag also plays a crucial role in genetic counselling, offering valuable advice on the risk of genetic conditions recurring within families. He assists individuals and couples in reproductive planning, providing insights and guidance for future pregnancies based on their genetic profiles. Moreover, he offers expert guidance on managing these conditions once a diagnosis is established.
Dr. Al-Shinnag holds prestigious fellowships with the Royal Australasian College of Physicians and the Human Genetics Society of Australasia. He serves as a staff specialist at the clinical genomics unit at St Vincent's Hospital Sydney. He completed physician training at the Royal Brisbane and Women's Hospital (RBWH) and advanced training in clinical genetics at Genetic Health Queensland across various hospitals.
The diagnostic genetics services offered by Dr. Al-Shinnag and his team include clinical assessments, investigation reviews, and genetic testing aimed at establishing accurate diagnoses. These diagnoses are instrumental in managing the conditions effectively and providing information to at-risk family members and those planning to expand their families.
Dr. Al-Shinnag's service specialises in addressing a range of conditions, some of which include congenital anomalies, intellectual disability, developmental delay, dysmorphic features, cardiac malformations and diseases, hearing loss, neurological and muscular disorders (such as genetic epilepsy, hereditary spastic paraparesis, peripheral neuropathy, and muscular dystrophy), and eye disorders (including retinitis pigmentosa, congenital cataract, early or late onset macular dystrophy, and various other retinal diseases).
“Evidence-based care tailored to each patient — taking the time to explain options and shared decisions.”
— Dr Mohammad Al-Shinnag
Opleiding & training
-
2000–2006 MD · Medicine and Surgery
-
2006–2010 Residency · Clinical Genetics
Carrière & aanstellingen
-
2010-09–2011-08 Junior consultant
Vergunningen & verzekering
Medische licenties
AU — Organización Médica Colegial de España (OMC)
Boardcertificeringen
European Board of Clinical Genetics
Beroepsaansprakelijkheidsverzekering:
Generali Healthcare · 3,000,000 EUR dekking · No claims on file
Uitgevoerde procedures
| Procedure | Code | Levenslang aantal |
|---|---|---|
| GP consultation | 99213 | 1,171 |
| Annual physical exam | 99395 | 1,421 |
| Vaccination administration | 90471 | 2,317 |
| Minor procedure (skin) | 17110 | 2,410 |
Diensten & prijzen
| Dienst | Duur | Modaliteit | Prijs |
|---|---|---|---|
| New patient consultation (60m) | 60 min | in_clinic|telemed | 180.00 EUR |
| Follow-up consultation (30m) | 30 min | in_clinic|telemed|phone | 90.00 EUR |
| Vaccination administration | 30 min | in_clinic | 450.00 EUR |
| Minor procedure (skin) | 120 min | in_clinic | 180.00 EUR |
Praktijk, team & in praktijk
Video's
Onderzoek & publicaties
h-index: 19 · i10: 13
-
Validation of clinical scoring in Clinical Genetics
DOI: 10.6300/euroclin.2026.0 · PMID: 35758536 · geciteerd door 83
-
Long-term follow-up of Clinical Genetics across AU
DOI: 10.5485/euroclin.2025.1 · PMID: 36758147 · geciteerd door 145
-
Validation of clinical scoring in Clinical Genetics
DOI: 10.9065/euroclin.2024.2 · PMID: 39282096 · geciteerd door 7
-
Long-term follow-up of Clinical Genetics across AU
DOI: 10.2970/euroclin.2023.3 · PMID: 37717592 · geciteerd door 109
Uitgenodigde lezingen
- Practical updates in Clinical Genetics European Annual Congress (Clinical Genetics) · Vienna · 2024 · invited
- Single-centre experience in Clinical Genetics National Society Meeting · Darlinghurst · 2023 · oral abstract
Onderscheidingen & lidmaatschappen
Onderscheidingen
- 🏆 Top-rated Clinical Genetics — Darlinghurst · EuroClinics Patient Choice · 2025 · regional
Lidmaatschappen
- WONCA Europe — Family Doctors — Member · Sinds 2011
- national college of family doctors — Member · Sinds 2011
- European Union of Medical Specialists (UEMS) — Member · Sinds 2011
Artikelen van deze arts
- Patient education Patient guide to Clinical Genetics
- Awareness When should you see a clinical genetics?
Voor internationale patiënten
- Coördinator
- Patient liaison · mohammad.al.shinnag@euroclinics.example
Locatie
1 tagPatiëntbeoordelingen
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Recente recensies
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★★★★★ ✓ Geverifieerd Very thorough first visit — explained every step. Booking was easy and the staff were welcoming.
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★★★★★ ✓ Geverifieerd Took time to listen and reviewed all my previous results. I would absolutely recommend.
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★★★★☆ ✓ Geverifieerd Professional and knowledgeable. Wait on the day was a bit long, otherwise excellent.
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