Causes of Clubfoot
Causes of Clubfoot (Diseases Database):
The follow list shows some of the possible medical causes of Clubfoot
that are listed by the Diseases Database:
Source: Diseases Database
Clubfoot Causes: Book Excerpts
Clubfoot as a symptom:
Conditions listing Clubfoot
as a symptom may also be potential underlying causes of Clubfoot.
Our database lists the following as having
Clubfoot as a symptom of that condition:
- 1q deletion
- 4p16.3 deletion
- Aase-Smith I syndrome
- Absent patellae - scrotal hypoplasia - renal anomalies - facial dysmorphism - mental retardation
- Acetaminophen - Teratogenic Agent
- Acro coxo mesomelic dysplasia
- Acrofacial dysostosis Preis type
- Acromesomelic dysplasia Brahimi Bacha type
- Adducted thumb syndrome recessive form
- Adducted thumbs - arthrogryposis, Christian type
- Adducted thumbs Dundar type
- Alajouanine syndrome
- Alprazolam - Teratogenic Agent
- Amobarbital - Teratogenic Agent
- Amoxicillin - Teratogenic Agent
- Ampola syndrome
- Amyotrophy, neurogenic scapuloperoneal, New England type
- Ankylosis - facial anomalies - pulmonary hypoplasia syndrome
- Annular constricting bands
- Arthrogryposis
- Arthrogryposis - severe scoliosis
- Arthrogryposis multiplex congenita neurogenic type
- Arthrogryposis multiplex congenita, distal, X-linked
- Arthrogryposis, congenital - myopathic seizures
- Ataxia - diabetes - goiter - gonadal insufficiency
- Atelosteogenesis Type III
- Atelosteogenesis, type 2
- Aureomycin - Teratogenic Agent
- Azathioprine - Teratogenic Agent
- Bangstad syndrome
- Baraitser burn fixen syndrome
- Benadryl - Teratogenic Agent
- Benzthiazide - Teratogenic Agent
- Biaxin - Teratogenic Agent
- Bird-headed dwarfism with progressive ataxia, Insulin-resistant diabetes, goiter and primary gonadal insufficiency
- Brachycephaly - deafness - cataract - mental retardation
- Brachycephaly - deafness - cataract - microstomia - mental retardation
- Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia
- Bruck syndrome
- Bruck syndrome, 2
- Campomelia Cumming type
- Campomelic dwarfism
- Campomelic dysplasia
- Camptodactyly syndrome, Guadalajara type 1
- Caudal dysplasia sequence
- Cerebellar atrophy with progressive microcephaly
- Cerebro oculo genital syndrome
- Cerebrocostomandibular Syndrome
- Cervical ribs, sprengel anomaly, anal atresia, urethral obstruction
- Charcot-Marie-Tooth disease, type 4
- Charcot-Marie-Tooth disease, Type 4B2
- Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma
- Chlorothiazide - Teratogenic Agent
- Chlorpromazine - Teratogenic Agent
- Chlortetracycline - Teratogenic Agent
- Chromosome 1, monosomy 1p32
- Chromosome 1, trisomy 1q42 qter
- Chromosome 10, trisomy 10p
- Chromosome 10p duplication syndrome
- Chromosome 10p duplication/10q deletion syndrome
- Chromosome 11q duplication syndrome
- Chromosome 13 ring syndrome
- Chromosome 13q deletion
- Chromosome 13q deletion syndrome
- Chromosome 14q, terminal duplication
- Chromosome 15, trisomy mosaicism
- Chromosome 15q duplication mosaicism
- Chromosome 17, deletion 17q23 q24
- Chromosome 18 deletion syndrome
- Chromosome 18 Ring
- Chromosome 18q, partial deletion
- Chromosome 19 ring syndrome
- Chromosome 19p duplication syndrome
- Chromosome 1q deletion
- Chromosome 21 monosomy
- Chromosome 21q deletion syndrome
- Chromosome 22, monosome mosaic
- Chromosome 22, monosomy mosaic
- Chromosome 3, trisomy 3p
- Chromosome 5q deletion syndrome
- Chromosome 6, monosomy 6q
- Chromosome 6q deletion syndrome
- Chromosome 7, trisomy 7p
- Chromosome 7p duplication syndrome
- Chromosome 8p inverted duplication syndrome
- Chromosome 9 trisomy syndrome
- Chromosome 9, trisomy
- Chromosome 9, Trisomy 9p (Multiple Variants)
- Chromosome diploid-triploid mosaicism syndrome
- Clarithromycin - Teratogenic Agent
- Clomiphene - Teratogenic Agent
- Clomocycline - Teratogenic Agent
- Clubfoot
- Cocaine - Teratogenic Agent
- Cortisone - Teratogenic Agent
- Crane-Heise syndrome
- Craniofacial dysostosis - arthrogryposis - progeroid appearence
- Crixan - Teratogenic Agent
- Cushing's symphalangism
- Cyclothiazide - Teratogenic Agent
- De Grouchy Syndrome
- Deal-Barratt-Dillon syndrome
- Declomycin - Teratogenic Agent
- Declostatin - Teratogenic Agent
- Del(1) (23-q25)
- Del(1) (q12-q21.3)
- Del(1) (q24-q25.3)
- Deletion 13q
- Deletion 18q
- Deletion 6q
- Demeclocycline - Teratogenic Agent
- Diastrophic dysplasia
- Dimedrol - Teratogenic Agent
- Diphenhydramine - Teratogenic Agent
- Distal arthrogryposis, Moore-Weaver type
- Disulfiram - Teratogenic Agent
- Diuril - Teratogenic Agent
- Doxycycline - Teratogenic Agent
- Duane-radial ray syndrome
- Dup (1) (q21.2-qter) and dup (14)(pter-q13)
- Dup (1)(pter-p31) and del(2)(q33-qter)
- Dup(1) (p31-p21)
- Duplication 10p
- Duplication 7p
- Dysplastic cortical hyperostosis
- Ecstacy - Teratogenic Agent
- Ectodermal dysplasia - arthrogryposis - diabetes mellitus
- Emanuel syndrome
- Ephedrine - Teratogenic Agent
- Epiphyseal dysplasia, multiple, 4
- Ergotamine - Teratogenic Agent
- Erythromycin - Teratogenic Agent
- Esophageal Atresia, Coloboma, Clubfoot
- Eye defects - arachnodactyly - cardiopathy
- Faciocardiomelic dysplasia, lethal
- Fanconi-ichthyosis-dysmorphism
- Femoral facial syndrome
- Femur-fibula-ulna syndrome
- Fenfluramine - Teratogenic Agent
- Fetal aminopterin syndrome
- Fibular hypoplasia or aplasia - femoral bowing - oligodactyly
- Fine-Lubinsky syndrome
- Frank-Ter Haar syndrome
- Freeman-Sheldon Syndrome
- Fried-Goldberg-Mundel syndrome
- Friedreich's ataxia
- Froster-Iskenius-Waterson syndrome
- Fryns-Fabry-Remans syndrome
- Fuhrmann syndrome
- Fuhrmann-Rieger-de Sousa syndrome
- Gentamicin - Teratogenic Agent
- Gordon Syndrome
- Hecht syndrome
- Herrmann Opitz arthrogryposis syndrome
- Hoon-Hall syndrome
- Humerospinal dysostosis - congenital heart disease
- Hydrochlorothiazide - Teratogenic Agent
- Hydrops ectrodactyly syndactyly
- Hypoplastic thumbs - hydranencephaly
- Idaho syndrome
- Imaizumi Kuroki syndrome
- Incontinentia Pigmenti
- Indigo Carmine - Teratogenic Agent
- Infex - Teratogenic Agent
- Insulin - Teratogenic Agent
- Isoproterenol - Teratogenic Agent
- Jequier-Kozlowski-skeletal dysplasia
- Klaricid - Teratogenic Agent
- Kosztolanyi syndrome
- Kozlowski Celermajer Tink syndrome
- Kozlowski-Celermajer syndrome
- Kurczynski-Casperson syndrome
- Lambert syndrome
- Lamotrigine - Teratogenic Agent
- Lateral body wall complex
- Le Marec-Bracq-Picaud syndrome
- Lederle - Teratogenic Agent
- Ledermycin - Teratogenic Agent
- Lethal chondrodysplasia, Moerman type
- Lissencephaly type III - metacarpal bone dysplasia
- Lithium - Teratogenic Agent
- Low birth weight - dwarfism - dysgammaglobulinemia
- Marden-Walker Syndrome
- Marden-Walker-like syndrome
- Massa-Casaer-Ceulemans syndrome
- MDMA - Teratogenic Agent
- Meckel Syndrome
- Megarbane syndrome
- Mental retardation - hip luxation - G6PD variant
- Mental retardation - unusual facies - talipes - hand anomalies
- Mental retardation unusual facies ampola type
- Mental retardation, Wolff type
- Methacycline - Teratogenic Agent
- Methocarbamol - Teratogenic Agent
- Methotrexate - Teratogenic Agent
- Methyclothiazide - Teratogenic Agent
- Metolazone - Teratogenic Agent
- Miconazole - Teratogenic Agent
- Microcephalic osteodysplastic dysplasia, Saul-Wilson type
- Microcephaly - seizures - mental retardation - heart disorders
- Mifepristone - Teratogenic Agent
- Minocycline - Teratogenic Agent
- Misoprostol - Teratogenic Agent
- Mobius syndrome
- Morse-Rawnsley-Sargent syndrome
- Multicore disease
- Multiple pterygium syndrome
- Nail-Patella Syndrome
- Nasopharyngeal teratoma with Dandy-Walker - diaphragmatic hernia
- Neomycin - Teratogenic Agent
- Nievergelt syndrome
- Nytol - Teratogenic Agent
- Omeprazole - Teratogenic Agent
- Opitz-Reynolds-Fitzgerald syndrome
- Opthalmo acromelic syndrome
- Oral facial digital syndrome, type 4
- Osteogenesis imperfecta - congenital joint contractures
- Otoonychoperoneal syndrome
- Oxytetracycline - Teratogenic Agent
- Papaverine - Teratogenic Agent
- Paramethadione - Teratogenic Agent
- Paroxetine - Teratogenic Agent
- Pelvic dysplasia arthrogryposis of lower limbs
- Penicillamine - Teratogenic Agent
- Penicillamine, D - Teratogenic Agent
- Peroxisomal bifunctional enzyme deficiency
- Phenylephrine - Teratogenic Agent
- Pitt-Hopkins syndrome
- Pizotifen - Teratogenic Agent
- Plum syndrome
- Polythiazide - Teratogenic Agent
- Prednisone - Teratogenic Agent
- Progestagen - Teratogenic Agent
- Prosencephaly - cerebellar dysgenesis
- Pseudoephedrine - Teratogenic Agent
- Quinethazone - Teratogenic Agent
- Radial defect - Robin sequence
- Radio digito - facial dysplasia
- Radio renal syndrome
- Ranitidine - Teratogenic Agent
- Ray-Peterson-Scott syndrome
- Renal dysplasia - limb defects syndrome
- Richieri-Costa-Silveira-Pereira syndrome
- Sacral agenesis
- Sandhaus Ben-Ami syndrome
- Sandrow syndrome
- Scapuloperoneal myopathy
- Scapuloperoneal syndrome, neurogenic type
- Scapuloperoneal syndrome, neurogenic, Kaeser type
- Schinzel Giedion Syndrome
- Seckel syndrome
- Seckel-like syndrome, type Buebel
- Short limb dwarfism, Al Gazali type
- Short stature - Robin sequence - cleft mandible - hand anomalies - clubfoot
- Short stature - talipes - natal teeth
- Shprintzen-Golberg craniosynostosis
- Simvastatin - Teratogenic Agent
- Skeletal dysplasia - mental retardation
- Smith-Lemli-Opitz syndrome, type 2
- Spinal Muscular Atrophy
- Spondylocostal dysostosis, Dandy-Walker
- Spondylocostal dysplasia dominant
- Spondyloepimetaphyseal dysplasia joint laxity
- Spondyloepimetaphyseal dysplasia with joint laxity
- Spondylohypoplasia arthrogryposis popliteal pterygium
- Spondylohypoplasia, arthrogryposis and popliteal pterygium
- Streptomycin - Teratogenic Agent
- Sulfasalazine - Teratogenic Agent
- Sulphasalazine - Teratogenic Agent
- Sumatriptan - Teratogenic Agent
- TAU syndrome
- Tel-Hashomer camptodactyly syndrome
- Terpin hydrate - Teratogenic Agent
- Tetracycline - Teratogenic Agent
- Tetraploidy
- Thiopropazate - Teratogenic Agent
- Thoracolimb dysplasia, Rivera type
- Tibia absent - polydactyly - arachnoid cyst
- Tolbutamide - Teratogenic Agent
- Triaminic - Teratogenic Agent
- Trichlormethiazide - Teratogenic Agent
- Trimethadione - Teratogenic Agent
- Triploid syndrome
- Trisomy 6
- VACTERL with hydrocephalus, X-linked
- Valproic Acid - Teratogenic Agent
- Varicella virus antenatal infection
- Vinblastine - Teratogenic Agent
- Vincristine - Teratogenic Agent
- Weaver like syndrome
- Weaver Syndrome
- X-linked mental retardation craniofacial abnormal microcepahly club
- X-linked mental retardation craniofacial abnormal microcephaly club
- Zellweger Syndrome
- Zidovudine - Teratogenic Agent
- Zuclopenthixol - Teratogenic Agent
Related information on causes of Clubfoot:
As with all medical conditions,
there may be many causal factors.
Further relevant information on causes of Clubfoot may be found in:
Causes of Clubfoot: Online Medical Books
16 MEDICAL BOOKS ONLINE!
Review excerpts from medical books online, free, without registration,
for more information about the causes of Clubfoot.
Clubbing:
Differential Diagnosis
(In A Page: Pediatric Signs and Symptoms)
-
Pulmonary
–Cystic fibrosis
–Bronchiectasis
–Empyema
–Pulmonary abscess
–Tuberculosis, aspergillosis
–Asthma complicated by infections
–Pulmonary alveolar proteinosis
–Sarcoidosis
–Interstitial pneumonitis (lymphoid, chronic)
–Pulmonary fibrosis
-
Cardiovascular
–Cyanotic congenital heart disease
–Congestive heart failure
–Myxoid tumor
–Subacute bacterial endocarditis
–Myxomas
-
Gastrointestinal
–Inflammatory bowel disease
–Gardner syndrome
–Parasitosis
–Biliary cirrhosis or biliary atresia
–Chronic active hepatitis
–Celiac disease
-
Other
–Diamond syndrome (myxedema, exophthalmos, clubbing)
–Thyrotoxicosis
–Hypervitaminosis A
–Malnutrition
-
Acquired, one or more digits
–Aortic/subclavian aneurysm
–Brachial plexus injury
–Shoulder subluxation
–Trauma
–Maffucci syndrome
–Gout
–Sarcoidosis
–Severe herpetic whitlow
-
Idiopathic
-
Hereditary, familial (isolated)
–Pachydermoperiostosis
-
Pseudoclubbing (broad distal phalanges with
normally shaped nails)
–Apert syndrome
–Pfeiffer syndrome
–Rubinstein-Taybi syndrome
» READ BOOK EXCERPT ONLINE »
Source: In A Page: Pediatric Signs and Symptoms, 2007
Clubbing:
Medical causes
(Handbook of Signs & Symptoms (Third Edition))
Bronchiectasis.
Clubbing commonly occurs in the late stage of bronchiectasis. Another classic sign is a cough that produces copious, foul-smelling, and mucopurulent sputum. Hemoptysis and coarse crackles over the affected area, heard during inspiration, are also characteristic. The patient may complain of weight loss, fatigue, weakness, and exertional dyspnea. He may also have rhonchi, fever, malaise, and halitosis.
Bronchitis.
With chronic bronchitis, clubbing may occur as a late sign and is unrelated to the severity of the disease. The patient has a chronic productive cough and may display barrel chest, dyspnea, wheezing, increased use of accessory muscles, cyanosis, tachypnea, crackles, scattered rhonchi, and prolonged expiration.
Emphysema.
Clubbing occurs late in emphysema. The patient may have anorexia, malaise, dyspnea, tachypnea, diminished breath sounds, peripheral cyanosis, and pursed-lip breathing. He may also display accessory muscle use, barrel chest, and a productive cough.
Endocarditis.
With subacute infective endocarditis, clubbing may be accompanied by a fever, anorexia, pallor, weakness, night sweats, fatigue, tachycardia, and weight loss. The patient may also develop arthralgia, petechiae, Osler's nodes, splinter hemorrhages, Janeway lesions, splenomegaly, and Roth's spots. Cardiac murmurs are usually present.
Heart failure.
Clubbing occurs as a late sign in heart failure along with wheezing, dyspnea, and fatigue. Other findings include jugular vein distention, hepatomegaly, tachypnea, palpitations, dependent edema, unexplained weight gain, nausea, anorexia, chest tightness, a slowed mental response, hypotension, diaphoresis, narrow pulse pressure, pallor, oliguria, a gallop rhythm (a third heart sound),and crackles on inspiration.
Interstitial fibrosis.
Clubbing usually occurs in the patient with advanced interstitial fibrosis. Typically, he also develops intermittent chest pain, dyspnea, crackles, fatigue, weight loss, and possible cyanosis.
Lung abscess.
Initially, lung abscess produces clubbing, which may reverse with resolution of the abscess. It can also cause pleuritic chest pain; dyspnea; crackles; a productive cough with a lot of purulent, foul-smelling, usually bloody sputum; and halitosis. The patient may also experience weakness, fatigue, anorexia, a headache, malaise, weight loss, and a fever with chills. You may hear decreased breath sounds.
Lung and pleural cancer.
Clubbing occurs commonly in lung and pleural cancers. Associated findings include hemoptysis, dyspnea, wheezing, chest pain, weight loss, anorexia, fatigue, and a fever.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Signs & Symptoms (Third Edition), 2006
Clubfoot:
Causes and incidence
(Professional Guide to Diseases (Eighth Edition))
A combination of genetic and environmental factors in utero appears to cause clubfoot. Heredity is a definite factor in some cases, although the mechanism of transmission is undetermined. In children without a family history of clubfoot, this anomaly seems linked to arrested development during the 9th and 10th weeks of embryonic life, when the feet are formed. Researchers also suspect muscle abnormalities, leading to variations in length and tendon insertions, as possible causes of clubfoot.
Clubfoot, which has an incidence of approximately 1 per 1,000 live births, usually occurs bilaterally and is twice as common in boys. It may be associated with other birth defects, such as myelomeningocele, spina bifida, and arthrogryposis.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Diseases (Eighth Edition), 2005
Clubbing:
Medical causes
(Professional Guide to Signs & Symptoms (Fifth Edition))
Bronchiectasis
Clubbing commonly occurs in the late stage of this disorder. Another classic sign is a cough producing copious, foul-smelling, and mucopurulent sputum. Hemoptysis and coarse crackles heard over the affected area during inspiration are also characteristic. The patient may complain of weight loss, fatigue, weakness, and exertional dyspnea. He may also have rhonchi, fever, malaise, and halitosis.
Bronchitis
Clubbing may occur as a late sign in chronic bronchitis, but it doesn’t reflect the severity of the disease. The patient has a chronic productive cough and may display barrel chest, dyspnea, wheezing, increased use of accessory muscles, cyanosis, tachypnea, crackles, scattered rhonchi, and prolonged expiration.
Emphysema
Clubbing occurs late in this disease, which may also cause anorexia, malaise, dyspnea, tachypnea, diminished breath sounds, peripheral cyanosis, pursed-lip breathing, accessory muscle use, barrel chest, and a productive cough.
Endocarditis
In subacute infective endocarditis, clubbing may be accompanied by fever, anorexia, pallor, weakness, night sweats, fatigue, tachycardia, and weight loss. The patient may also develop arthralgia, petechiae, Osler’s nodes, splinter hemorrhages, Janeway lesions, splenomegaly, and Roth’s spots. Cardiac murmurs are usually present.
Heart failure
Clubbing is a late sign of heart failure along with wheezing, dyspnea, and fatigue. Other findings include jugular vein distention, hepatomegaly, tachypnea, palpitations, dependent edema, unexplained weight gain, nausea, anorexia, chest tightness, slowed mental response, hypotension, diaphoresis, narrow pulse pressure, pallor, oliguria, a gallop rhythm (a third heart sound),and crackles on inspiration.
Interstitial fibrosis
Clubbing occurs in almost all patients with advanced interstitial fibrosis. Typically, the patient also develops intermittent chest pain, dyspnea, crackles, fatigue, weight loss and, possibly, cyanosis.
Lung abscess
Initially, this disorder produces clubbing, which may resolve with resolution of the abscess. It can also cause pleuritic chest pain, dyspnea, crackles, halitosis, and a productive cough with a large amount of purulent, foul-smelling, and commonly bloody sputum. The patient may also experience weakness, fatigue, anorexia, headache, malaise, weight loss, and fever with chills. Auscultation may reveal decreased breath sounds.
Lung and pleural cancer
Clubbing occurs commonly in these cancers. Associated findings include hemoptysis, dyspnea, wheezing, chest pain, weight loss, anorexia, fatigue, and fever.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006
Nail Phenomena/Clubbing:
Differential Overview
(Field Guide to Bedside Diagnosis)
Phenomena
❑ Pitting
❑ Transverse depression
❑ Transverse white line
❑ Nailfold telangiectasias
❑ Nailfold infarcts
❑ Splinter hemorrhages
❑ Onycholysis
❑ Spoon nails
❑ Blue-green nails
❑ White nails
❑ Half-and-half nails
❑ Yellow nails
❑ Blue lunulae
❑ Red lunulae
❑ Black longitudinal streak
Clubbing
❑ Bronchogenic cancer
❑ Tuberculosis
❑ Endocarditis
❑ Inflammatory bowel disease
❑ Familial
❑ Trauma
❑ Grave disease
❑ Cirrhosis
❑ Cystic fibrosis
❑ Cyanotic congenital heart disease
❑ Pulmonary fibrosis
❑ Mediastinal Hodgkin disease
❑ Mesothelioma
❑ Lung abscess
❑ Bronchiectasis
❑ Hypertrophic osteoarthropathy
❑ Pachydermoperiostosis
» READ BOOK EXCERPT ONLINE »
Source: Field Guide to Bedside Diagnosis, 2007
Clubfoot:
Causes
(Handbook of Diseases)
A combination of genetic and environmental factors in utero appears to cause clubfoot. Heredity is a definite factor in some cases, although the mechanism of transmission is undetermined. If a child is born with clubfoot, his sibling has a 1 in 35 chance of being born with the same anomaly. Children of a parent with clubfoot have 1 chance in 10.
In children without a family history of clubfoot, this anomaly seems linked to arrested development during the 9th and 10th weeks of embryonic life, when the feet are formed. Researchers also suspect muscle abnormalities, leading to variations in length and tendon insertions, as possible causes of clubfoot.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Diseases, 2003
Clubbing:
Medical causes
(Nursing: Interpreting Signs and Symptoms)
Bronchiectasis.Clubbing commonly occurs in the late stage of bronchiectasis. Another classic sign is a cough that produces copious, foul-smelling, and mucopurulent sputum. Hemoptysis and coarse crackles over the affected area, heard during inspiration, are also characteristic. The patient may complain of weight loss, fatigue, weakness, and exertional dyspnea. He may also have rhonchi, fever, malaise, and halitosis.
Bronchitis.With chronic bronchitis, clubbing may occur as a late sign and is unrelated to the severity of the disease. The patient has a chronic productive cough and may display barrel chest, dyspnea, wheezing, increased use of accessory muscles, cyanosis, tachypnea, crackles, scattered rhonchi, and prolonged expiration.
Emphysema.Clubbing occurs late in emphysema. The patient may have anorexia, malaise, dyspnea, tachypnea, diminished breath sounds, peripheral cyanosis, and pursed-lip breathing. He may also display accessory muscle use, barrel chest, and a productive cough.
Endocarditis.With subacute infective endocarditis, clubbing may be accompanied by a fever, anorexia, pallor, weakness, night sweats, fatigue, tachycardia, and weight loss. The patient may also develop arthralgia, petechiae, Osler's nodes, splinter hemorrhages, Janeway lesions, splenomegaly, and Roth's spots. Cardiac murmurs are usually present.
Heart failure.Clubbing occurs as a late sign in heart failure along with wheezing, dyspnea, and fatigue. Other findings include jugular vein distention, hepatomegaly, tachypnea, palpitations, dependent edema, unexplained weight gain, nausea, anorexia, chest tightness, a slowed mental response, hypotension, diaphoresis, narrow pulse pressure, pallor, oliguria, a gallop rhythm (a third heart sound),and crackles on inspiration.
Interstitial fibrosis.Clubbing usually occurs in the patient with advanced interstitial fibrosis. Typically, he also develops intermittent chest pain, dyspnea, crackles, fatigue, weight loss, and possible cyanosis.
Lung abscess.Initially, a lung abscess produces clubbing, which may reverse with resolution of the abscess. It can also cause pleuritic chest pain; dyspnea; crackles; a productive cough with a lot of purulent, foul-smelling, usually bloody sputum; and halitosis. The patient may also experience weakness, fatigue, anorexia, a headache, malaise, weight loss, and a fever with chills. You may hear decreased breath sounds.
Lung and pleural cancer.Clubbing occurs commonly in lung and pleural cancers. Associated findings include hemoptysis, dyspnea, wheezing, chest pain, weight loss, anorexia, fatigue, and a fever.
» READ BOOK EXCERPT ONLINE »
Source: Nursing: Interpreting Signs and Symptoms, 2007
Clubfoot:
Clubfoot - pathophysiology
(The 5-Minute Pediatric Consult)
- Many anatomic abnormalities have been postulated as causing clubfoot:
- Anomalous or deficient muscles, myoblasts, mast cells, abnormal primary bone formation, joint and muscle contractures, vascular anomalies (absent dorsalis pedis artery), nerve anomalies
- Abnormalities of the fibrous connective tissue
- Interruption of the development of the embryonic foot has also been suggested.
Clubfoot - etiology
- Most cases are idiopathic (multifactorial inheritance pattern with significant environmental influence).
- Infrequently, neuromuscular imbalance may underlie the deformity (cerebral palsy, myelomeningocele, lipomas of the cord, caudal or sacral agenesis, polio, arthrogryposis, fetal alcohol syndrome).
» READ BOOK EXCERPT ONLINE »
Source: The 5-Minute Pediatric Consult, 2008
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