FBHH

(redirected from Familial Benign)
AcronymDefinition
FBHHFamilial Benign (Hypocalciuric) Hypercalcaemia
FBHHFull Bandwidth at Half Height (neurophysiological research)
References in periodicals archive ?
Familial benign hypocalciuric hypercalcemia (FBHH) is a benign situation which develops due to inactivating mutation of calcium sensing receptor (CaSR).
Hailey-Hailey Disease (HHD: MIM 169600) was first described by Hailey brothers in 1939.1 HHD is also known as familial benign chronic pemphigus.
DISCUSSION: Hailey-Hailey disease also known as familial benign chronic pemphigus is a relatively uncommon disease in India.
"Familial benign chronic pemphigus" by Hailey and Hailey, April 1939.
Familial benign chronic pemphigus (Hailey-Hailey disease).
Familial benign pemphigus is a chronic autosomal dominant disorder with incomplete penetrance, which manifests clinically as vesicles and erythematous plaques with overlying crusts, which typically occur in the genital area, as well as the chest, neck, and axillary areas.
Familial benign chronic pemphigus, also known as Hailey-Hailey disease, is an uncommon autosomal dominant genetic condition.
Caption: Familial benign chronic pemphigus lesions commonly affect the neck, axillae, and flexures.
Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemia.
Axillary hyperhidrosis, apocrine bromhidrosis, hidradenitis suppurativa, and familial benign pemphigus: surgical approach.
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