Feeding Your Baby with Cleft Palate
Information and advice about how to ensure proper nutrition and manage feeding difficulties that affect many babies with cleft lip and palate.
Caring for your child
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Showing 1 - 10 of 15 results
March of Dimes
March of Dimes is an international organization that works to prevent birth defects, premature birth, and infant mortality and to support expectant and new parents.
Living with XXY
A blog by Ryan Bregante about what it means to live with Klinefelter syndrome, also known as 47 XXY, including helpful resources, personal stories, local meetings and much more.
Association for X and Y Variations (AXYS)
AXYS is an advocacy, education and support organization for individuals with X and Y chromosome variations and their families.
American Society of Plastic Surgeons (ASPS)
The American Society of Plastic Surgeons (ASPS) offers information about cleft lip and cleft palate repairs.
Cleft Advocate
The Cleft Advocate educates and inspires families whose lives are touched by cleft lip and/or palate or other craniofacial anomalies.
AdoptCleft
AdoptCleft is a support group for parents wanting to adopt cleft children, parents that have cleft children (biological or adopted), and others that can contribute or learn from the conversations.
American Cleft Palate-Craniofacial Association (ACPA)
ACPA is an international nonprofit medical society of healthcare professionals who treat and/or perform research on birth defects of the head and face.
Diagnosis and Treatment of Cleft Lip and Palate
In this video, clinicians and patient families talk about the diagnosis and treatment of cleft lip and palate, the most common congenital facial anomaly.
Genetics Home Reference — Beckwith-Wiedemann syndrome
The Genetics Home Reference is an online guide from the National Institutes of Health designed to help you understand genetic conditions. It includes a handbook, glossary and resources.