Pediatric & Genetic Diseases_Panel
The multidisciplinary team of pediatricians, geneticists, genetic counselors, and allied health professionals collaborate. It provides compassionate care, comprehensive diagnostics, and personalized treatment plans for children with genetic conditions. Here’s why it is essential to prioritize pediatric and genetic health and how Lifecode can help:
Why Prioritize Pediatric & Genetic Health:
- Early Intervention: Many genetic diseases and pediatric conditions benefit from early intervention and treatment. Identifying genetic disorders and pediatric diseases as early as possible. It shall allow for timely intervention, symptom management, and proactive measures to optimize developmental outcomes.
- Family Planning: Understanding the genetic risks and implications of inherited conditions is crucial for family planning decisions. Genetic testing and counseling can further provide valuable information to families about the likelihood of passing on genetic disorders. It shall help them make informed decisions about reproductive options and prenatal care.
- Precision Medicine: Advances in genetic testing and personalized medicine have revolutionized the diagnosis and treatment of genetic diseases. Tailoring treatment plans to an individual’s genetic makeup allows for more targeted and effective therapies. It shall reduce the burden of symptoms and improve the quality of life for patients with genetic conditions.
- Preventive Care: Genetic screening and counseling can further identify individuals at increased risk for certain genetic diseases. This shall allow for proactive measures like lifestyle modifications, surveillance, and preventive interventions. This shall lower the likelihood of disease development or progression.
Lifecode’s Approach to Pediatric & Genetic Diseases:
- Comprehensive Evaluation: Lifecode offers comprehensive evaluations including medical history review, physical examination, genetic testing, imaging studies, and laboratory tests. It helps in diagnosing and characterizing genetic disorders and pediatric conditions accurately.
- Genetic Counseling: The healthcare provides genetic counseling services to individuals and families affected by genetic conditions. Our certified genetic counselors offer personalized support, education, and guidance to help families understand. The genetic basis of their condition, navigate treatment options and make informed decisions about their health and future.
- Multidisciplinary Care: Lifecode’s multidisciplinary team collaborates shall develop individualized treatment plans tailored to each child’s unique needs, preferences, and goals. The team shall include geneticists, pediatric specialists, pediatric surgeons, nutritionists, developmental specialists, and therapists. They shall all work together to provide comprehensive care and support.
- Research and Innovation: It is actively involved in research and innovation to advance the understanding and treatment of pediatric and genetic diseases. Participation in clinical trials and collaborative research initiatives shall all help in offering cutting-edge therapies, investigational treatments, and novel interventions to patients.
Why Choose Lifecode for Pediatric & Genetic Disease Care:
- Expertise and Experience: The team of pediatric specialists, geneticists, and allied health professionals are known to be leaders in the field of pediatric and genetic medicine. With specialized training, expertise, and experience. We further deliver compassionate, evidence-based care to children and families affected by genetic disorders.
- State-of-the-Art Facilities: The healthcare is equipped with advanced diagnostic technology, genetic testing laboratories, pediatric clinics, and pediatric specialties. It shall be about units to provide comprehensive care for pediatric and genetic diseases.
- Family-Centered Care: Lifecode is well committed to providing family-centered care with a focus on communication, collaboration, and support. We partner with families to develop personalized treatment plans that address their unique needs, values, and goals.
- Holistic Approach: Lifecode shall take a holistic approach to pediatric and genetic disease care. This shall address not only the medical aspects of the condition but also the social, emotional, and developmental needs of the child and family.
Prioritizing pediatric and genetic health is essential for early intervention, personalized treatment, and improved outcomes for children and families affected by genetic disorders and pediatric conditions. With Lifecode’s comprehensive approach to pediatric and genetic disease care, you can trust that your child’s health and well-being are in good hands.
| Categories | Conditions Observed |
|---|---|
Allergies | Allergic Rhinitis |
| Allergies in General |
| Allergy to Pets |
| Allergy to mites |
| Allergy to pollen |
| Asthma |
| Atopic Dermatitis |
| Cockroach allergy |
| Contact dermatitis |
| Eczema |
| Egg White Allergy |
| Grass allergy |
| Histamine Intolerance |
| Milk Allergy |
| Peanut Allergy |
| Sensitivity to secondhand smoke |
|
|
Auditory system | Non-syndromic deafness |
| Otitis |
|
|
Behavioral Changes | Aggressiveness |
| Neuroticism |
|
|
Benefits | Optimism Trend |
|
|
Cancer | Childhood Leukemia |
| Retinoblastoma |
|
|
Cardiovascular | Aortic stenosis |
| Cardiac Arrhythmia |
| Cardiovascular Disease (Cholesterol Level) |
| Familial Hyperlipoproteinemia Type III |
| Hereditary familial hypercholesterolemia |
| Hypercholesterolemia (Type B) |
|
|
Dentistry | Caries |
| Periodontitis |
| Teeth development |
|
|
Diabetes | Early Type 2 Diabetes |
| Type 1 Diabetes |
| Type 2 diabetes |
|
|
Digestive system | Canker sores |
| Cystic fibrosis |
|
|
Drug Reactions | Vaccine Reactions |
|
|
Endocrine system | Hashimoto’s Thyroiditis |
| Hashimoto’s Thyroiditis (in children) |
| Hypothyroidism |
|
|
General | Aversion to Vegetables and Coffee |
| Bacterial Meningitis |
| Williams Syndrome |
|
|
Genetic diseases | Angelman Syndrome |
| Blepharophimosis Syndrome |
| Char syndrome |
| Cockayne’s Syndrome |
| Hyperornithinemia-Hyperammonemia-Homocitrulinuria Syndrome |
| Kabuki Syndrome |
| Marfan syndrome |
| Miller-Dieker Syndrome |
| Mucopolysaccharidosis Type VI |
| PANDAS Syndrome |
| Phelan-McDermid Syndrome |
| Prader-Willi Syndrome |
| Rett Syndrome |
| Smith-Magenis Syndrome |
| Treacher-Collins Syndrome |
| Type 0B Glycogenosis |
| Ubiquitins |
|
|
Hematologic system | Anemia |
| HDL (Cholesterol) |
| Hemolytic Anemia |
| Low ferritin in children under 2 years |
| Spherocytosis |
| Triglycerides |
|
|
Hormone | Folic Acid Metabolism |
| Growth Hormone (GH) Deficiency |
|
|
Hormones | Aromatase Deficiency |
|
|
Immune system | Allergy to Food Colors |
| Chronic adenoiditis |
| HLA-DQ2.2 |
| HLA-DQ2.5 |
| HLA-DQ4 |
| HLA-DQ7 |
| HLA-DQ8 |
| Tonsillitis |
|
|
Internalizations | Anxiety |
| Depression |
| Internalizing Disorder |
|
|
Metabolic | Celiac disease |
| Lactose intolerance |
| Methylenetetrahydrofolate reductase (MTHFR) deficiency |
| Obesity |
| Trend of Eating Sweets |
|
|
Metabolic disorders | Cerebrotendinous Xanthomatosis (CTX) |
|
|
Muscular system | Becker Muscular Dystrophy |
| Dystonia |
|
|
Need for Nutrients | Iodine |
|
|
Neurological | Motor coordination |
| Rolandic Epilepsy |
| West syndrome |
|
|
Pains | Headache |
|
|
Pediatric | Delayed Motor Development |
| Neonatal Mortality |
|
|
Personal characteristics | Attention deficit |
| Circadian Rhythm Impact |
| Cognitive Flexibility |
| Cognitive empathy |
| Creativity |
| Greater Stimulus with Caffeine |
| Height |
| Hyperactivity |
| Increased Environmental Sensitivity |
| Manual dexterity |
| Memory |
| Memory (long term, logic) |
| Memory (traumatic) |
| Memory (verbal) |
| Obsessive-Compulsive Disorder (OCD) |
| Physical resistance |
| Sense of Taste (Bitter) |
| Skill in Mathematics |
| Sociability |
| Susceptibility to Bacteria |
| Tendency to sleep late |
| Visuospatial Working Memory |
| Worst Social Interaction in Autism |
| Worst Verbal Communication in Autism |
|
|
Provocative | Oppositional defiant disorder (ODD) |
|
|
Psychiatric | Addiction tendency (eating, gambling, alcohol, smoking) |
| Anorexia Nervosa |
| Attention Deficit Hyperactivity Disorder (ADHD) |
| Autism (Asperger’s Syndrome) |
| Autism Spectrum Disorder (ASD) |
| Autism Visual Endophenotype |
| Cataplexy and Narcolepsy (sleep) |
| Cognitive skills, attention and memory |
| Dyslexia |
| Face Recognition Memory |
| Intelligence (higher IQ if breastfed) |
| Intelligence – IQ |
| Language disorder |
| Motion sickness |
| Non-syndromic Intellectual Disability |
| Openness to New Experiences |
| RBFOX1 gene |
| Restless Legs Syndrome (Willis-Ekbom disease) |
| Shyness |
| Type A Personality |
| Type D Personality |
|
|
Reproductive system | Male precocious puberty |
|
|
Respiratory system | Interstitial Lung Disease |
| Respiratory Syncytial Virus (RSV) |
|
|
Skeletal system (bones) | Atelosteogenesis |
| Hypochondroplasia |
| Musculoskeletal Pain |
| Scoliosis |
|
|
Skin | Acne |
|
|
Urinary system | Chronic Kidney Disease |
| Nephroliathiasis in children |
| Nephrotic syndrome |
| Renal agenesis |
| Smaller Kidneys in Newborns |
|
|
Vision (Ophthalmology) | Astigmatism |
| Myopia |
|
|
Vitamins | Vitamin D |
|
|
Vitamins need | Biotinidase Deficiency |
|
|
Weight | Binge Eating Disorder |
| Obesity in Adolescents |
What Is The Pediatric & Genetic Diseases Panel?
The pediatric & genetic diseases panel is a specialized diagnostic tool designed to assess genetic markers and biomarkers associated with a wide range of pediatric and genetic disorders, offering comprehensive insights into the underlying causes of childhood diseases.
How Does The Panel Aid In Diagnosing Pediatric Diseases?
The panel utilizes advanced genetic testing techniques to analyze specific genetic variants and biomarkers related to pediatric conditions, facilitating early diagnosis, personalized treatment planning, and improved outcomes for children.
Who Should Consider Undergoing The Pediatric & Genetic Diseases Panel?
Parents with children experiencing unexplained symptoms, developmental delays, or A family history of genetic disorders may benefit from this panel to uncover underlying genetic causes and guide appropriate medical management.
What Information Does The Panel Provide About Pediatric Diseases?
The panel offers insights into A wide range of pediatric conditions, including metabolic disorders, neurological conditions, congenital anomalies, and rare genetic syndromes, enabling targeted interventions and personalized care plans for affected children.
Can The Panel Predict The Likelihood Of Inherited Diseases In Children?
While not definitive, the panel’s analysis of genetic markers and biomarkers can provide valuable information about the risk of inherited diseases in children, aiding in early detection, prevention, and family planning decisions.
