Birth Defects reported by Pfizer
To June 2022, Pfizer reported 1,143 "Congenital, familial and genetic disorders" with "Preferred Terms". I list them and ask about "1p36 Deletion Syndrome" mentioned, then mysteriously disappeared.
"1p36 Deletion Syndrome" was the first mentioned in the famous Post-marketing Report of Adverse Events “of Special Interest” released under Court Order decades ahead of the company’s plans.1
The Report was approved by the US FDA on 30 April 2021 and I was one of the first to get a copy, being part of the team assembled waiting for Public Health and Medical Professionals for Transparency posting material as soon as it became available.2
In subsequent reports, this "1p36 Deletion Syndrome" was obviously edited out.
What good are lists? - many will say. I think it is easier to focus on a condensed list of tragic "Congenital, familial and Genetic Disorders" with "Preferred Terms" as reported by the jab profiteers themselves, with all the built-in redundancy and euphemisms as printed. Pity the Mums and Dads as well as the deformed Children.
Picture credit.3
Looking at the June 2022 document of 393 pages4 listing Adverse Events we see:
Aberrant aortic arch; Abnormal palmar/plantar creases; Absence of cranial vault; Accessory muscle; Accessory spleen; Acquired gene mutation; Acral peeling skin syndrome; Acrodermatitis enteropathica; Adenomatous polyposis coli; Adrenogenital syndrome; Adrenoleukodystrophy; Alpha-1 antitrypsin deficiency; Amegakaryocytic thrombocytopenia; Amputation; Amyotrophic lateral sclerosis gene carrier; Anal atresia; Anencephaly; Ankyloglossia; Anomaly; Anodontia; Anomalous pulmonary venous connection; Anophthalmos; Anotia; Antithrombin III deficiency; Aorta hypoplasia; Aortic stenosis; Aplasia; Aplasia cutis congenita; Arachnodactyly; Argininosuccinate synthetase deficiency; Arnold-Chiari malformation; Arrhythmogenic right ventricular dysplasia; Arterial malformation; Arterial tortuosity syndrome; Arteriovenous malformation; ASAH1 related disorder; Asplenia; Asymmetric crying facies; Ataxia telangiectasia; Atrial septal defect; Atrioventricular septal defect; Auditory neuropathy spectrum disorder; Autoimmune lymphoproliterative syndrome; Autism spectrum disorder (listed under Psychiatric Disorders)
Benign familial haematuria; Benign familial pemphigus; Bicuspid aortic valve; Biliary hamartoma; Birth mark; Blindness; Block vertebra; Brachydactyly; Brachyolmia; BRAF gene mutation; Brain malformation; Branchial cyst; Breast malformation; Brugada syndrome;
CADASIL; Cancer gene carrier; Cardiac septal defect; Cardiovascular anomaly; Carnitine palmitoyltransferase deficiency; Cataract; Caudal regression syndrome; Central nervous system anomaly; Cerebellar hypoplasia; Cerebral arteriovenous malformation haemorrhagic; Cerebral cavernous malformation; Cerebral palsy; Cerebrovascular anomaly; Cerebrovascular arteriovenous malformation; Chimerism; Chordee; Chronic granulomatous disease; Cleft lip; Cleft lip and palate; Cleft palate; Cleft uvula; Clinodactyly; Cloacal exstrophy; Coarctation of the aorta; Colour blindness; Combined immunodeficiency; Comeal dystrophy; Cortical dysplasia; Craniosynostosis; Cryopyrin associated periodic syndrome; Cryptorchism; CYP2C19 polymorphism; Cystic fibrosis; Cystic kidney disease; Cystic lung; Cystic lymphangioma; Cytogenetic abnormality; Cytomegalovirus infection;
Dacryostenosis; Dermoid cyst; Developmental hip dysplasia; Diaphragmatic hernia; Diastematomyelia; Diastrophic dysplasia; Dolichocolon; Double inlet left ventricle; Double outlet right ventricle; Ductus arteriosus premature closure; Dysmorphism;
Ectopic thyroid; Ectrodactyly; Ehlers-Danlos syndrome; Elliptocytosis hereditary; Encephalocele; Epidermolysis bullosa; Exomphalos; Eye disorder;
Factor II mutation; Factor IX deficiency; Factor V deficiency; Factor VII deficiency; Factor VIII deficiency; Factor V Leiden mutation; Factor X deficiency; Factor XI deficiency; Factor XI11 deficiency; Fallot's tetralogy; Familial amyotrophic lateral sclerosis; Familial hemiplegic migraine; Familial mediterranean fever; Familial periodic paralysis; Familial tremor; Fibrodysplasia ossificans progressiva; Foetal chromosome abnormality; Foetal cystic hygroma; Foetal malformation; Foramen magnum stenosis; Foot malformation; Friedreich's ataxia;
Gastrointestinal malformation; Gastroschisis; Gene mutation; Gilbert's syndrome; Glucose-6-phosphate dehydrogenase deficiency, Glycogen storage disease type V; Glycogen storage disorder; Great vessel anomaly; Grey matter heterotopia;
Haematological disorder; Haemophilia; Haemorrhagic arteriovenous malformation; Heart disease congenital; Hand malformation; Hamartoma; Heart valve disorder; Hereditary angioedema; Hereditary angioedema with normal C1 esterase inhibitor; Hereditary ataxia; Hereditary fructose intolerance; Hereditary haemorrhagic telangiectasia; Hereditary motor and sensory neuropathy; Hereditary neuropathy with liability to pressure palsies; Hereditary optic atrophy; Hereditary spherocytosis; Heterotaxia; Homocystinaemia; Huntington's disease; Hydrocephalus; Hydranencephaly; Hydrocele; Hydronephrosis; Hypercoagulation; Hyperexplexia; Hyperglycinaemia; Hyper IgD syndrome; Hypertrophic cardiomyopathy; Hypochondroplasia, Hypophosphatasia; Hypoplastic left heart syndrome;
Ichthyosis; Imperforate oesophagus; Inborn error of metabolism; Intestinal atresia; Intracranial lipoma; Isodicentric chromosome 15 syndrome;
Janus kinase 2 mutation; Jaw malformation;
Keams-Sayre syndrome; Keratosis follicular; Kidney duplex; Kidney malformation; Klippel-Trenaunay syndrome;
Laryngomalacia; Left-to-right cardiac shunt; Limb hypoplasia congenital; Limb reduction defect; Long QT syndrome congenital; Low set ears; LUMBAR syndrome;
Macrocephaly; Macroglossia; Malformation venous; MELAS syndrome; Melkersson-Rosenthal syndrome; Meningocele; Meningomyelocele; Metabolic myopathy; Methaemoglobinaemia; Methylenetetrahydrofolate reductase gene mutation; Microcephaly; Micrognathia; Micropenis; Microphthalmos; Mitochondrial encephalomyopathy; Mitochondrial myopathy; Mitral valve atresia; Mitral valve incompetence; Moebius II syndrome; Multiple congenital abnormalities; Muscular dystrophy; Musculoskeletal disorder; Musculoskeletal disorder of limbs; Musculoskeletal disorder of skull; Musculoskeletal disorder of spine; Myasthenic syndrome; Myocardial bridging; Myoclonic dystonia; Myoclonic epilepsy and ragged-red fibres; Myopathy; Myotonic dystrophy;
Naevus flammeus; Nail aplasia; Neonatal alloimmune thrombocytopenia; Neonatal haemochromatosis; Neurofibromatosis; Neurological degeneration; Non-compaction cardiomyopathy; Nose malformation; Nystagmus;
Odontogenic cyst; Optic nerve anomaly; Oral malformation; Osteogenesis imperfecta;
Pachyonychia congenita; Pancreas divisum; Parkes-Webersyndrome; Paroxysmal extreme pain disorder; Pectus excavatum; Penoscrotal fusion; Persistent foetal circulation; Pfeiffer syndrome; Phelan-McDermid syndrome; Phimosis; Platybasia; Polycystic liver disease; Polydactyly; Polymicrogyria; Porencephaly; Porokeratosis; Porphyria; Porphyria acute; Porphyria non-acute; Potter’s syndrome; Preauricularcyst; Primary ciliary dyskinesia; Protein C deficiency; PTEN gene mutation; Pulmonary artery stenosis; Pulmonary hypoplasia; Pulmonary malformation; Pulmonary sequestration; Pulmonary valve stenosis;
Rathke's cleft cyst; Renal aplasia; Renal dysplasia; Renal fusion anomaly; Retinitis pigmentosa; Right-to-left cardiac shunt; Rippling muscle disease; RUNX1 gene mutation
Schizencephaly; Scimitar syndrome; Sensory neuropathy; Short-chain acyl-coenzyme A dehydrogenase deficiency; Sickle cell anaemia; Sickle cell disease; Single atrium; Single umbilical artery; Skeletal dysplasia; Skin dimples; Skin malformation; Spina bifida; Spinal muscular atrophy; Spinal vessel congenital anomaly; Stargardt’s disease; Sturge-Weber syndrome; Supernumerary nipple; Syndactyly; Syringomyelia;
Talipes; Telangiectasia congenital; Thalassaemia; Thalassaemia minor; Thyroglossal cyst; Tourette’s disorder; Tracheo-oesophageal fistula; Transposition of the great vessels; Tricuspid valve atresia; Trisomy 8; Trisomy 13; Trisomy 16; Trisomy 18; Trisomy 21; Turner's syndrome; Type IIa hyperlipidaemia; Type V hyperlipidaemia;
Univentricular heart; Urachal abnormality; Urethral atresia; Urethral valves;
VACTERL syndrome; Vascular endothelial growth factor overexpression; Vascular malformation; Venous angioma of brain; Ventricular hypoplasia; Ventricular septal defect; Vertebral artery hypoplasia; Vestibulocerebellar syndrome; VEXAS syndrome; Von Willebrand's disease;
Williams syndrome; Wolf-Hirschhom syndrome,
X-linked lymphoproliferative syndrome; XXX syndrome
Compare with “Non Interventional Study”
Pfizer is running a study on an unknown number of Unjabbed people. To June 2022, that group reported 34 Birth Defects compared to the Jabbed 1,143.
See also my report that counted 376 different types of Birth Defect to April 2022.
This in turn links to related reports, which are updated as new information appears.
See also
January 2024 Update
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