Abidi Syndrome - Causes, Symptoms, Diagnosis, and Treatment
Abidi syndrome is a rare genetic disorder. Read the article below to know more about it.
Dr. Devanga Manjushree Selvaraj
09 Apr 2024 . 4 min read
Benign Recurrent Intrahepatic Cholestasis and Its Genetics
Benign recurrent intrahepatic cholestasis is a rare disorder inherited through autosomal recessive patterns. Continue reading to know more about this condition.
26 Dec 2023 . 4 min read
Chromosome 2p Duplication Syndrome
It is a genetic condition that causes developmental delay, behavioral problems, and distinct facial features. Read the article to know more.
12 Apr 2024 . 5 min read
Translocation - Its Types, Mechanism, and Its Biological Significance
Translocation is the process by which a piece of a gene moves from one location to another inside a cell's genome or between different cells or organisms.
26 Feb 2024 . 4 min read
Pulmonary Genetic Program and Its Management
Primary genetic programs help to identify peculiar genes that cause different lung problems. Read to know more.
02 Jan 2024 . 4 min read
Precision Medicine and Genomics in Pediatrics: A Revolution in Children's Healthcare
Precision medicine and genomics offer personalized approaches that consider a child's unique genetic makeup, lifestyle, and environment.
24 Jan 2024 . 4 min read
Cellular Aging - Definition and Causes
Growing old makes the cell age. Let us know about this biological fact in the article below.
01 Feb 2024 . 4 min read
Type XI Glycogen Storage Disease/Fanconi-Bickel Syndrome
Fanconi-Bickel syndrome, or type XI storage disease, is a congenital disorder that disrupts glucose transport. It is a rare condition. Read the article to know more.
22 Dec 2023 . 5 min read
ATR-X Syndrome - From Gene Mutation to Clinical Presentation
ATR-X syndrome is an X-chromosome-linked rare genetic disorder that causes intellectual and hematological dysfunctions.
13 Feb 2024 . 5 min read
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