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The signs and symptoms of branchio-oto-renal syndrome are consistent with underdeveloped (hypoplastic) or absent kidneys with resultant chronic kidney disease or kidney failure. Ear anomalies include extra openings in front of the ears, extra pieces of skin in front of the ears (preauricular tags ), or further malformation or absence of the ...
The clinical features of TBS overlap with VATER and VACTERL associations, oculo-auriculo-vertebral (OAV) spectrum, branchio-oto-renal (BOR) syndrome, and Fanconi anemia and other 'anus-hand-ear' syndromes. [4] Although some symptoms can be life-threatening, many people diagnosed with Townes-Brocks Syndrome live a normal lifespan. [2]
Branchio-oto-renal syndrome; C. Cardiorenal syndrome; Cardiovascular–kidney–metabolic syndrome; Cat eye syndrome; Childhood-onset nephrotic syndrome;
However, if skin pits are found on both sides of the neck, then, branchio-oto-renal syndrome should be ruled out. Infection of the cysts in this region can compress trachea , causing respiratory problems, or it can compress the oesophagus , causing dysphagia , and irritating the sternocleidomastoid muscle, causing torticollis .
Renal dysplasia is a type of familial kidney disease characterized by abnormal cellular differentiation of kidney tissue. Dogs and cats with kidney disease caused by these diseases have the typical symptoms of kidney failure, including weight loss, loss of appetite, depression, and increased water consumption and urination. [ 1 ]
Brachycephalic airway obstructive syndrome; Brainstem stroke syndrome; Branchio-oculo-facial syndrome; Branchio-oto-renal syndrome; Bromism; Brown's syndrome; Brown-Séquard syndrome; Brown–Vialetto–Van Laere syndrome; Bruck syndrome; Brugada syndrome; Brunner syndrome; Budd–Chiari syndrome; Burning feet syndrome; Burning mouth syndrome ...
Shaker syndrome in dogs is a condition that primarily affects small breeds and can be very concerning for owners. When your dog is shaking or shivering more than normal, it can be tempting to ...
Branchio-oculo-facial syndrome (BOFS) [1] is a disease that arises from a mutation in the TFAP2A gene. It is a rare autosomal dominant disorder that starts to affect a child's development before birth. [ 1 ]