About Genetic Disorders for NEET SS
Genetic Disorders entails studying a wide range of medical conditions caused by abnormalities or mutations in an individual's genes. You can enhance your preparation for NEET SS pediatrics by utilizing study resources inclusive of conceptual video lectures aligned with comprehensive notes, Mock Test Series, QBank, etc.
Access Genetic Disorders for Your Preparation
An Overview Of Genetic Skin Disorders
Genodermatoses are a heterogeneous institution of genetic issues that usually affect the skin, mucosa, hair, and now and again nails. These situa...
Read MoreApr 16 2024
Noonan Syndrome : Epidemiology, Genes Implicated, Clinical Manifestations, Treatment
This syndrome, which affects both boys and females, has a normal karyotype but phenotypically resembles Turner syndrome.Epidemiology Of Noonan Sy...
Read MoreApr 04 2024
Image Based Questions On Genetics
Mitochondrial InheritanceAll children born to a mother are affected suggesting mitochondrial inheritance.Fragile X-syndromeTrinucleotide repeat d...
Read MoreMar 20 2024
How does PrepLadder make Genetic Disorders learning easy for students?
At PrepLadder, we ensure a seamless and effective preparation experience for NEET SS aspirants with our conceptual video lectures aligned with comprehensive notes, for an in-depth understanding of the most complex topics.
Meet our Genetic Disorders Faculty
An experienced teacher, Dr. Sandeep Sharma has been teaching NEET-PG, NEET-SS and FMGE students for the past 8 years both in India and abroad. He is a subject expert in General Medicine, Medicine Gastroenterology, Medicine Hepatology and Medicine Oncology. After completing his MBBS and MD in Medicine from PGI Chandigarh. He is currently working as a Consultant Pediatrician at Omni Clinics and Diagnostics, Sector 34, Chandigarh.
Latest Articles
Pediatric Epilepsy Syndromes with Favourable and Unfavourable Outcome
Pediatric Epilepsy Syndrome, which have a good outcome, are further grouped into groups as follows:Neonatal onsetBenign Neonatal Convulsions or Benign
What is Paroxysmal Nocturnal Hemoglobinuria?
Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare blood disorder in children. It is an acquired disorder due to somatic mutations affecting hematoge
Congenital and Acquired Hypothyroidism in Children
Thyroid Development and FunctionThe thyroid gland arises as an outpouching of the foregut near the base of the tongue, also called the foramen caecum.
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