is a rare genetic condition causing eye, pituitary, and developmental abnormalities.

causes developmental delay, speech and learning difficulties, sometimes seizures and congenital anomalies.

is a rare chromosome 14 duplication causing developmental delays and congenital anomalies.

is a chromosome 15q duplication (extra copy) causing overgrowth and developmental delays.

involves a small missing chromosome piece causing variable developmental and learning challenges.

is a genetic condition causing developmental delays, autism-like features, seizures, hypotonia.

is a genetic change causing variable development, learning, seizures, and behavior differences.

is a rare chromosome 15q14 deletion causing developmental delays and learning differences.

is a genetic condition from missing 15q24 DNA, causing developmental delays.

is a genetic condition causing developmental delays, learning differences, and variable features.

is a chromosomal duplication causing variable developmental, learning, and behavioral differences.

is a rare genetic condition causing developmental delays and variable physical differences.

is a genetic deletion causing variable developmental delays, learning issues, seizures.

is a small extra DNA segment with variable developmental and behavioral effects.

is a rare chromosomal change causing variable development, learning, and growth differences.

is a rare chromosomal deletion causing developmental delays and congenital anomalies.

is a rare microdeletion on chromosome 16 causing developmental delays and anomalies.

is a genetic condition from extra 17p11.2 DNA causing developmental delays.

causes extra genetic material, leading to developmental delays and variable features.

is a 17q11 chromosome deletion causing neurofibromatosis-related skin, nerve, learning challenges.

is a chromosome 17 microduplication causing variable developmental and behavioral differences.

is a genetic condition with variable kidney, diabetes, and developmental differences.

involves duplication of 17q12, causing variable developmental, behavioral, and kidney features.

is a rare genetic disorder causing developmental delay, hypotonia, learning difficulties.