The Ministry of Health and Prevention (MoHAP) held a coordination meeting with representatives from private hospitals to ...

Objective Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is an inherited adrenal steroid synthesis ...

New Jersey can continue retaining dried blood spots obtained under a newborn screening program after a federal court rejected claims the retention policy is unconstitutional.

Infants up to 6 weeks old with genetically diagnosed presymptomatic spinal muscular atrophy (SMA) treated with oral risdiplam ...

The country's first fully dedicated, facility-integrated Newborn Screening Continuity Clinic (NBSCC) was inaugurated at the ...

Starting on August 1st, the Wisconsin newborn screening program will be adding two genetic disorders X-ALD and MPS type 1 to their panel.

Spinal muscular atrophy (SMA) is a genetic neuromuscular disease affecting specialized nerve cells that control voluntary ...

MONDAY, Aug. 11, 2025 (HealthDay News) — Spinal muscular atrophy (SMA) is a genetic neuromuscular disease affecting ...

We spoke with Neil Ward from PacBio about England’s plan to introduce whole genome sequencing for every newborn, and how long-read technology is shaping the future of early diagnosis around the world.

Overview of the Market  The global Cystic Fibrosis Market is valued at USD 10.3 Billion in 2024 and is projected to reach a ...

Hearing loss in children often goes unnoticed—but early detection can make all the difference. Discover the signs, causes, ...