Acromelanosis is a condition that causes dark patches of skin pigmentation. It is a congenital condition, which means it is present from birth or appe...

Acromelic dysplasia is a group of skeletal disorders that affect bone growth and development, with several recognized subtypes described, including fo...

Acromelic frontonasal dysostosis is a rare form of frontonasal dysplasia. This condition is marked by a combination of distinct craniofacial, brain, a...

Acromesomelic dysplasia is a very rare, inherited condition that affects the bones and leads to a form of short-limb dwarfism. This condition is chara...

Acromesomelic dysplasia 1, Maroteaux type is a rare genetic condition that affects the growth of bones. It is characterized by severe dwarfism with an...

Acromesomelic dysplasia 2A is a rare genetic condition that affects bone development. This condition mainly causes severe dwarfism at birth with abnor...

Acromesomelic dysplasia 2B, also known as Du Pan syndrome, fibular hypoplasia and complex brachydactyly, or fibular aplasia-complex brachydactyly synd...

Acromesomelic dysplasia, Hunter-Thompson type is a rare genetic condition that leads to severe dwarfism, with adult height around 120 cm. People with...

Acromesomelic dysplasia 3 is a rare condition that affects skeletal development. It is also known by several other names, including AMDD and Demirhan...

Acromesomelic dysplasia 4 (AMD4) is a rare skeletal condition that primarily affects the growth of the long bones in the limbs. Although detailed desc...

acromesomelic dysplasia, Campailla Martinelli type is a rare disease. Detailed information about this condition is currently limited in medical litera...

Acromicric dysplasia is a rare skeletal disorder characterized by short stature, short hands and feet, and mild facial dysmorphism, with distinctive X...

Acroosteolysis is a rare condition characterized by the degeneration of the distal phalanges, which are the bones at the tips of the fingers. This pro...

Acroosteolysis dominant type is a rare genetic condition that affects the bones. This condition is known for the loss of bone tissue in the fingertips...

Acroosteolysis-keloid-like lesions-premature aging syndrome is a rare condition that has been reported under several names, including premature ageing...

Acrootoocular syndrome is a very rare condition characterized by pseudopapilledema, mixed hearing loss, distinctive facial features, and limb extremit...

Acro-pectoral syndrome is a rare condition that affects the limbs and the upper part of the chest. People with this condition have abnormalities in th...

Acro-pectoro-renal field defect is a very rare condition that involves a combination of physical features affecting the chest, hands, and kidneys. Thi...

Acropectorovertebral dysplasia is a skeletal dysplasia characterized by fusion of the carpal and tarsal bones along with complex anomalies of the fing...

Acro-renal-mandibular syndrome is a very rare condition that causes multiple congenital anomalies. People with this syndrome may have differences in t...