Sturge–Weber syndrome, sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder.

Homozygous leopards are substantially more prone to congenital stationary night blindness.

Congenital stationary night blindness is present at birth and is characterized by impaired vision in dark conditions.

Also, the "Haab scale" is a device used to measure pupillary diameter, and "Haab's striae" are horizontal breaks in the Descemet membrane associated with congenital glaucoma.

Most cases are acquired, although some children are born with a congenital short bowel.

Sullavan suffered from the congenital hearing defect otosclerosis that worsened as she aged, making her more and more hard of hearing.

She has the visual disability of oculocutaneous albinism, a congenital vision impairment, and is . , Blow is attending the University of Sydney and double majoring in Arts and Education, which would enable her to become an English and drama teacher.

Young–Simpson syndrome (YSS), is a rare congenital disorder with symptoms including hypothyroidism, heart defects, facial dysmorphism, cryptorchidism in males, hypotonia, mental retardation and postnatal growth retardation.

In 1950 Bruce joined the University of Washington, where he continued research on the single-stage test, particularly as a predictor of the success of surgery for valvular or congenital heart disease.

There is a high degree of congenital deafness among the Ka'apor, and consequently most of the hearing community knows sign language.

Because of the increased risk of infection, physicians administer oral antibiotics as a prophylaxis after a surgical splenectomy (or starting at birth, for congenital asplenia or functional asplenia).

This can be congenital (genetic disorder) or it can develop later, as in the case of aplastic anemia or some kinds of leukemia.

MORM syndrome is an autosomal recessive congenital disorder characterized by mental retardation, truncal obesity, retinal dystrophy, and micropenis".

Entropion is usually caused by genetic factors and very rarely it may be congenital when an extra fold of skin grows with the lower eyelid (epiblepharon).

Congenital cases are also seen with the brachicephalic breeds being over represented.

Tricuspid atresia is a form of congenital heart disease whereby there is a complete absence of the tricuspid valve.

When they are poisoned by "C. maculatum" during the fetus's organ formation period, the offspring is born with malformations, mainly palatoschisis and multiple congenital contractures (MCC; frequently described as arthrogryposis).

Additionally, she was born with Ebstein malformation, a congenital heart defect, agenesis of the corpus callosum, and hip dysplasia.

The disorder may be congenital (existing at or before birth), or acquired.

Because this syndrome can be acquired or occur at random and has spontaneous resolution, Brown hypothesized one major truth for this disorder — that the short tendon sheath was due to a complete separation, congenital paresis, of the ipsilateral (on the same side) inferior oblique muscle and secondary to a permanent shortening.

After further research, he redefined the sheath syndrome into the following divisions: true sheath syndrome, which categorized only the cases that had a congenital short anterior sheath of the superior oblique tendon, and simulated sheath syndrome, which characterized all cases in which the clinical features of a sheath syndrome caused by something different other than a congenital short anterior sheath of the tendon.

The clinical features of the two categories are correct but true sheath syndrome is always congenital. However, in 1970 it was discovered that a tight sheath tendon was not the cause of Brown's Syndrome.

Mobius syndrome - a rare congenital disorder in which both VIth and VIIth nerves are bilaterally affected giving rise to a typically 'expressionless' face.

During this tour, Backstreet Boys member Brian Littrell underwent surgery to correct a congenital heart defect he had had since birth.

Congenital amputation is a congenital disorder that can be caused by fibrous bands of the amnion that constrict foetal limbs to such an extent that they fall off due to missing blood supply.

Congenital amputations can result from a number of causes.

The term "congenital amputation" is sometimes used loosely to mean "congenital absence".

Dinosaur eggs may have been the victim of the same causes of mortality suffered by modern bird and reptile eggs, like asphyxiation due to overly deep burial, congenital health problems, dehydration, disease, drowning, and inimical temperatures.

He had a congenital eye disease however, which cut his cinematography career short.

Homozygosity for "GCK" alleles with reduced function can cause severe congenital insulin deficiency, resulting in persistent neonatal diabetes.

This creates hypoglycemia of varying patterns, including transient or persistent congenital hyperinsulinism, or fasting or reactive hypoglycemia appearing at an older age.

Polysplenia is a congenital disease manifested by multiple small accessory spleens.

There are frequent associated congenital anomalies all related to deviations in the development of anatomical asymmetries in early embryonic stages.

Associated conditions include heterotaxy syndrome, intestinal malrotation, situs inversus, biliary atresia, and the range of congenital cardiac malformations most commonly dextrocardia, atrial situs ambiguus, ventricular inversion, and VA concordance with left posterior aorta.

SCD has become the most common genetic disease in the country, with an overall birth prevalence of 1/2,415 in mainland France, ahead of phenylketonuria (1/10,862), congenital hypothyroidism (1/3,132), congenital adrenal hyperplasia (1/19,008) and cystic fibrosis (1/5,014) for the same reference period.

Research on the development of the syndrome suggest that congenital heart disease is typically present at an early age, often at the infant's first pediatric appointment.

Among the more reliable features suggestive of Williams are congenital heart disease, periorbital fullness ("puffy" eyes), and the presence of a long smooth philtrum.

Collie eye anomaly (CEA) is a congenital, inherited, bilateral eye disease of dogs, which affects the retina, choroid, and sclera.

These actions are not considered to be chucking as they are due to the distinctive architecture of their elbows, possibly a congenital condition.

Several congenital disorders of glycosylation are associated with mutations in enzymes involved in mannose metabolism.

A different project has connected the cytoplasmic multi-PDZ domain protein GRIP1, an interaction partner of Eph/ephrin proteins and other molecules, with the rare but severe human congenital disease Fraser Syndrome.