Author

Ana Rosales Page 9

At an academic children’s hospital, Ana Rosales, CGC, LGC, works with physicians evaluating dysmorphology and unexplained pediatric conditions. She spent years as a clinical research coordinator in pediatric cardiology before training in medical genetics. Rosales spends clinic days reviewing diagnostic testing options, discussing inheritance patterns with parents, and drafting informational resources for patients facing unexpected results. Rosales works closely with laboratory geneticists to interpret ambiguous variants and assess clinical relevance for children with multisystem disorders.

The L1CAM Gene and Its Role in L1 Syndrome Genetics
What a KCNQ2 Gene Mutation Means for Child Development Genetics
Homocystinuria: Causes, Symptoms, and Treatment Genetics
Neonatal Marfan Syndrome: Signs, Diagnosis, and Prognosis Kids
Simpson-Golabi-Behmel Syndrome: Causes, Symptoms & Risks Genetics
Trisomy 9p: Causes, Characteristics, and Diagnosis Genetics
Trisomy 4: Causes, Types, and Prognosis Genetics
Neonatal Progeria: Causes, Signs, and Diagnosis Kids
What Is Waardenburg Syndrome Type 4?Genetics
What Are 1q21 Deletion and Duplication Syndromes?Genetics
What Is SETD5 Syndrome and How Is It Diagnosed?Genetics
Trisomy 1: Causes, Types, and Fetal Impact Genetics
Farber Disease: Causes, Symptoms, and Diagnosis Immunity
Saethre-Chotzen Syndrome: Causes, Symptoms & Treatment Genetics
Mucolipidosis: Causes, Symptoms, Types, and Diagnosis Genetics
Argininosuccinic Aciduria: Causes, Symptoms, and Treatment Genetics
What Is Penta X Syndrome? A Look at This Rare Condition Genetics
What Is the FOXP1 Gene and FOXP1 Syndrome?Genetics
Mowat-Wilson Syndrome: Symptoms, Genetics, and Diagnosis Genetics
What Is EEC Syndrome? A Guide to this Genetic Condition Genetics
CHARGE Syndrome in Adults: A Look at Daily Life Genetics
Vici Syndrome: Causes, Symptoms, and Long-Term Outlook Genetics
Currarino Syndrome: Causes, Symptoms, and Prognosis Gut & Kidney
What Are 6q Chromosome Deletions and Duplications?Genetics
WDR4 Gene Mutations and Galloway-Mowat Syndrome Genetics
MED13L Syndrome: Causes, Symptoms, and Life With It Genetics
Female Facial Features of Fragile X Syndrome Genetics
What Is a Pericentric Inversion and What Are the Risks?Genetics
Monosomy 18: Causes, Symptoms, and Diagnosis Genetics
ELP1 Gene: Function and Role in Familial Dysautonomia Genetics