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Hallermann Streiff syndrome

The Hallermann-Streiff syndrome (also known as the François Dyscephalic Syndrome, Hallermann-Streiff-François syndrome, Oculomandibulodyscephaly with hypotrichosis and the Oculomandibulofacial Syndrome) is a disorder that effects the body's stature, head structure and hair growth. Patients with this syndrome are shorter than the average person and may not develop hair in many places, including in the facial, leg and pubic areas. Many patients also have problems with teeth growing enough or only develop one set of teeth in their lifetime. Eye problems may include clouded or reduced eye size. more...

Hairy cell leukemia
Hallermann Streiff syndrome
Hallux valgus
Hantavirus pulmonary...
HARD syndrome
Harlequin type ichthyosis
Hartnup disease
Hashimoto's thyroiditis
Hearing impairment
Hearing loss
Heart block
Heavy metal poisoning
HELLP syndrome
Hemifacial microsomia
Hemolytic-uremic syndrome
Hemophilia A
Hemorrhagic fever
Hepatic encephalopathy
Hepatitis A
Hepatitis B
Hepatitis C
Hepatitis D
Hepatocellular carcinoma
Hepatorenal syndrome
Hereditary amyloidosis
Hereditary angioedema
Hereditary ataxia
Hereditary ceroid...
Hereditary coproporphyria
Hereditary elliptocytosis
Hereditary fructose...
Hereditary hemochromatosis
Hereditary hemorrhagic...
Hereditary spastic...
Hereditary spherocytosis
Hermansky-Pudlak syndrome
Herpes zoster
Herpes zoster oticus
Hidradenitis suppurativa
Hip dysplasia
Hirschsprung's disease
Hodgkin lymphoma
Hodgkin's disease
Horner's syndrome
Horseshoe kidney
Howell-Evans syndrome
Human parvovirus B19...
Hunter syndrome
Huntington's disease
Hurler syndrome
Hutchinson Gilford...
Hutchinson-Gilford syndrome
Hydatidiform mole
Hydrops fetalis
Hypereosinophilic syndrome
Hyperimmunoglobinemia D...
Hyperkalemic periodic...
Hyperlipoproteinemia type I
Hyperlipoproteinemia type II
Hyperlipoproteinemia type...
Hyperlipoproteinemia type IV
Hyperlipoproteinemia type V
Hypertensive retinopathy
Hypertrophic cardiomyopathy
Hypokalemic periodic...
Hypoplastic left heart...
Hypothalamic dysfunction

There are less than 200 people with that syndrome worldwide. An organisation supporting people with the Hallermann Streiff Syndrome is the Germany based "Schattenkinder e.V."


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Diagnosis of Stridor in Children
From American Family Physician, 11/15/99 by Alexander K.C. Leung

Stridor is a sign of upper airway obstruction. In children, laryngomalacia is the most common cause of chronic stridor, while croup is the most common cause of acute stridor. Generally, an inspiratory stridor suggests airway obstruction above the glottis while an expiratory stridor is indicative of obstruction in the lower trachea. A biphasic stridor suggests a glottic or subglottic lesion. Laryngeal lesions often result in voice changes. A child with extrinsic airway obstruction usually hyperextends the neck. The airway should be established immediately in children with severe respiratory distress. Treatment of stridor should be directed at the underlying cause. (Am Fam Physician 1999;60:2289-96.)

The word "stridor" is derived from the Latin word "stridulus," which means creaking, whistling or grating. Stridor is a harsh, vibratory sound of variable pitch caused by partial obstruction of the respiratory passages that results in turbulent airflow through the airway. Although stridor may be the result of a relatively benign process, it may also be the first sign of a serious and even life-threatening disorder. Stridor is a distressing symptom to its victims and their parents, and presents a diagnostic challenge to physicians. As such, stridor demands immediate attention and thorough evaluation to uncover the precise underlying cause. This article reviews the etiology of stridor in children and suggests an approach to evaluating and managing the problem.

Etiology and Clinical Manifestations

Causes of stridor in children according to the site of obstruction are listed in Table 1.


Choanal Atresia. Choanal atresia, although rare, is the most common congenital anomaly of the nose. Choanal atresia results from a persistence of the bucconasal membrane in the posterior nares at the posterior margin of the hard palate. Unilateral choanal atresia does not usually cause any clinical problem unless the contralateral side is obstructed, for example, as a result of an upper respiratory tract infection. Bilateral choanal atresia is a life- threatening condition and a well-recognized cause of airway obstruction and respiratory distress in the newborn.

Lingual Thyroid or Thyroglossal Cyst. A lingual thyroid is due to a failure of descent of the thyroid gland. A thyroglossal cyst arises from remnants of the thyroglossal duct.

Clinically, a thyroglossal cyst presents as a smooth, discrete mass in the midline of the neck anywhere from just above the hyoid bone to the thyroid gland. Typically, the mass moves upward when the tongue is protruded. A lingual thyroid or thyroglossal cyst, if large enough, may cause airway obstruction and stridor.

Macroglossia. Macroglossia may result from Beckwith-Wiedemann syndrome, Down syndrome, glycogen storage disease and congenital hypothyroidism. The tongue may be large enough to obstruct the hypopharynx.

Micrognathia. Obstruction of the oropharynx may result from micrognathia by posterior displacement of the tongue. The obstruction typically worsens in the supine position as gravity pulls the tongue farther back.(1) Micrognathia is a classic feature of Pierre-Robin syndrome (Figure 1), Treacher Collins syndrome and Hallermann-Streiff syndrome.

Hypertrophic Tonsils/Adenoids. Tonsillar or adenoidal tissue may be so large that the supraglottic airway becomes obstructed. Characteristically, the stridor is most noticeable during sleep.

Retropharyngeal or Peritonsillar Abscess. A retropharyngeal or peritonsillar abscess may cause stridor as edema of the hypopharynx develops. Although both may present with fever, drooling and dysphagia, the child with a peritonsillar abscess may have difficulty opening the mouth (trismus) because of spasm of the pterygoid muscles, while the child with a retropharyngeal abscess often keeps the neck hyperextended.


Laryngomalacia. Laryngomalacia is the most common cause of chronic stridor in children younger than two years. It has a male-to-female ratio of approximately 2:1.(1) The condition is due to an intrinsic defect or delayed maturation of supporting structures of the larynx. The airway is partially obstructed during inspiration by the prolapse of the flaccid epiglottis, arytenoids and aryepiglottic folds. The inspiratory stridor is usually worse when the child is in a supine position, when crying or agitated, or when an upper respiratory tract infection occurs.(2)

Laryngeal Web, Cyst or Laryngocele. A laryngeal web results from a failure of the embryonic airway to recanalize.(3) Most laryngeal webs occur at the level of the vocal cords and are anterior in location.(3) A laryngeal cyst typically occurs in the aryepiglottic fold or in the epiglottis. A laryngeal cyst usually contains mucus from minor salivary glands. A laryngocele arises as a dilatation of the saccule of the laryngeal ventricle. A laryngeal web, cyst or laryngocele may present with stridor, usually at birth or soon after.

Laryngotracheobronchitis (Viral Croup). The most common cause of acute stridor in childhood is laryngotracheobronchitis, or viral croup. The condition is caused most commonly by parainfluenza virus, but it can also be caused by influenza virus types A or B, respiratory syncytial virus and rhinoviruses.(4) Croup usually occurs in children six months to six years of age, with a peak incidence in the second year of life. The male-to-female ratio is approximately 3:2.(4) Croup is usually preceded by an upper respiratory tract infection of several days' duration. A low-grade fever, barking cough, inspiratory stridor and hoarseness then develop. Symptoms are characteristically worse at night and are aggravated by agitation and crying.

Acute Spasmodic Laryngitis (Spasmodic Croup). Spasmodic croup may mimic laryngotracheobronchitis, except that it is usually not preceded by an upper respiratory tract infection, and it often occurs with a sudden onset at night. Allergy, psychologic factors and gastroesophageal reflux may trigger spasmodic croup. Spasmodic croup may be recurrent.

Epiglottitis. In children, epiglottitis is almost always caused by Haemophilus influenzae type b.(5) In recent years, the occurrence of epiglottitis has been reduced dramatically by the widespread use of the H. influenzae type b vaccine.(5) Epiglottitis usually occurs in children two to seven years of age, with a peak incidence in three-year- olds.(6)

The male-to-female ratio is approximately 3:2. The disease is characterized by an abrupt onset of high fever, toxicity, agitation, stridor, dyspnea, muffled voice, dysphagia and drooling. The older child may prefer to sit leaning forward with the mouth open and the tongue somewhat protruding. There is no spontaneous cough. An edematous, cherry red epiglottis, visualized in a controlled environment, is the hallmark of epiglottitis.

Vocal Cord Paralysis. Unilateral vocal cord paralysis occurs more often on the left side because of the longer course of the recurrent laryngeal nerve, which makes it more vulnerable to injury. Unilateral dysfunction may result from birth trauma, trauma during thoracic surgery or compression by mediastinal masses of cardiac, pulmonary, esophageal, thyroid or lymphoid origin. Bilateral vocal cord paralysis is more commonly associated with central nervous system problems including perinatal asphyxia, cerebral hemorrhage, hydrocephalus, bulbar injury and Arnold-Chiari malformation.(1) The vocal cords may also be injured by direct trauma from endotracheal intubation attempts or during deep airway suction. In vocal cord paralysis, the stridor is typically biphasic. In unilateral vocal cord paralysis, the infant's cry is weak and feeble; however, there is usually no respiratory distress. In bilateral vocal cord paralysis, the voice is usually of good quality, but there is marked respiratory distress.(3)

Laryngotracheal Stenosis. Laryngotracheal stenosis is a congenital or acquired narrowing of the airway representing a continuum of disease that may affect the glottis, subglottis and trachea.(7) The term "subglottic stenosis" was often used incorrectly in the past.(7) The most common cause of acquired laryngotracheal stenosis is endotracheal intubation, especially in low-birth-weight infants who require prolonged intubation and ventilation. Other causes include blunt trauma to the neck, high tracheotomy, cricothyrotomy, external compression of the airway and gastroesophageal reflux.(7)

Intubation. Intubation may result in vocal cord paralysis, laryngotracheal stenosis, subglottic edema and laryngospasm. Any of the above, alone or in combination, may lead to airway obstruction and stridor.

Foreign Body. Foreign body aspiration is a common cause of acute stridor. The peak incidence is between one and two years of age.

The foreign body is usually food. A history of aspiration or choking can be obtained in 90 percent of cases. The most common symptoms of laryngotracheal foreign bodies are cough, stridor and dyspnea, whereas those of bronchial foreign bodies are cough, decreased breath sounds, wheezing and dysphagia. Stridor may occur because of direct compression of the trachea by large objects lodged in the postcricoid region, paraesophageal inflammation, abscess formation or direct extension of the inflammatory process into the trachea by ulceration and fistula formation.

Cystic Hygroma. A cystic hygroma is a collection of lymphatic sacs that contain clear, colorless lymph. The lesion is congenital and probably represents a cluster of lymph channels that failed to connect into the normal lymphatic pathway. It commonly occurs in the neck area (Figure 2). The tumor, as it grows, may cause tracheal compression and stridor.

Subglottic Hemangioma. A subglottic hemangioma occurs more commonly in girls, with a female-to-male ratio of 2:1.(8) The lesion is usually submucosal. No color change or, at most, a slight bluish discoloration is evident. It is frequently associated with hemangiomas elsewhere on the body. The stridor is biphasic and exaggerated by crying or straining as the lesion tends to become engorged.(8)

Laryngeal Papilloma. This is the most common laryngeal neoplasm in children and usually results from vertical transmission of human papillomavirus at birth. Usually multiple, papillomas most commonly occur in the vocal cords and ventricular bands but can involve any part of the larynx. They are most common in children between two and four years of age. The usual presenting symptom is hoarseness, but some patients have stridor and other signs of laryngeal obstruction.

Angioneurotic Edema. Angioneurotic edema may result in acute swelling of the upper airway with resultant stridor and dyspnea. Swelling of the face, tongue or pharynx may also be present.

Laryngospasm (Hypocalcemic Tetany). Hypocalcemia may rarely cause laryngospasm and stridor.(9) Other features include irritability, tremors, twitchings and carpopedal spasm.

Psychogenic Stridor. Stridor may be caused by emotional stress or it may be a manifestation of a conversion disorder. Vocal cord malfunction associated with emotional stress may result in inspiratory or expiratory stridor.(10)

Characteristically, the onset of stridor is sudden but without the expected amount of distress. The neck is often held in a flexed position rather than in an extended position.


Tracheomalacia. Tracheomalacia is characterized by abnormal tracheal collapse secondary to inadequate cartilaginous and myoelastic elements supporting the trachea. Tracheal narrowing occurs with expiration and causes stridor.(11) The stridor may not be present at birth but appears insidiously after the first weeks of life. The stridor is usually aggravated by respiratory tract infections and agitation.(11)

Bacterial Tracheitis. Bacterial tracheitis is usually caused by Staphylococcus aureus, although it can also be caused by H. influenzae type b and Moraxella catarrhalis. Most patients are younger than three years of age. Bacterial tracheitis usually follows an upper respiratory tract infection. The patient then becomes seriously ill with high fever, toxicity and respiratory distress.

External Compression. Tracheal compression may result from vascular anomalies such as double aortic arch, right aortic arch with left ligamentum arteriosum, anomalous innominate artery, anomalous left common carotid artery, anomalous left pulmonary artery or aberrant subclavian artery. The child may prefer to keep the neck hyperextended. The stridor resulting from tracheal compression is often aggravated by feeding.

The trachea may also be compressed by a mediastinal cyst, teratoma, lymphoma or lymphadenopathy.

Clinical Evaluation

A thorough history (Table 2) and physical examination (Table 3) are important in the evaluation of children with stridor. Figure 3 presents an algorithm helpful in evaluating stridor in children.

Diagnostic Studies

Anteroposterior and lateral radiographic views of the neck are useful in the assessment of adenoidal and tonsillar size, epiglottic size and shape, retropharyngeal profile and subglottic and tracheal anatomy.(12) High-kilovoltage technique is preferable because it gives better visualization of the soft tissue. The lateral neck radiograph must be taken with good extension of the neck and during inspiration so that the pharyngeal soft tissues are not mistaken for a retropharyngeal mass.(13) Anteroposterior and lateral views of the chest are useful in the detection of radio-opaque foreign body and concomitant pulmonary disease. If foreign body aspiration is suspected and the preliminary films are negative, inspiratory and expiratory films should be obtained to look for air trapping behind the foreign body, producing a hyperlucent lung field in the ipsilateral side and a shift of the mediastinum to the opposite side.

A barium swallow is a useful method if vascular compression or gastroesophageal reflux is suspected. Gastrografin should be used as the contrast medium if tracheoesophageal fistula is suspected. Videofluoroscopy is useful in the diagnosis of tracheomalacia, foreign body aspiration and vocal cord dysfunction. Computed tomographic (CT) scan and magnetic resonance imaging (MRI) may be obtained to visualize the airway and the surrounding soft tissue structures, including any evidence of vascular compression.

Direct examination of the airway is often necessary to confirm the diagnosis and is essential in children with persistent stridor. Flexible fiberoptic bronchoscopy is widely used in the evaluation of airways in children. However, rigid bronchoscopy performed under general anesthesia gives a better view of the airway, especially the part below the level of the vocal cords. Rigid bronchoscopy also allows tissue biopsy and removal of foreign bodies using forceps.

A complete blood count is useful if an infection is suspected. Determination of the erythrocyte sedimentation rate is helpful in assessing for the presence of an infection. Depending on the degree of respiratory distress, arterial blood gas determination may be necessary to assess the degree of hypoxia and ventilatory status. An electrocardiogram and echocardiogram are indicated if significant heart murmurs are present or when structural heart disease is suspected.


Treatment of stridor should be directed at the underlying cause.

The airway should be established immediately in children with severe respiratory distress or actual airway obstruction. This can be done by endotracheal intubation. After adequate ventilation is achieved by intubation, tracheostomy can be performed if deemed necessary. Supportive measures may include oxygen, humidified air, intravenous fluids, suction and aerosol treatments with steroids and beta-adrenergic drugs.

The authors thank Dianne Leung for expert secretarial assistance and Sulakhan Chopra of the University of Calgary Medical Library for assistance in the preparation of the manuscript.

ALEXANDER K.C. LEUNG, M.B.B.S., is clinical associate professor of pediatrics at the University of Calgary, a pediatric consultant at the Alberta Children's Hospital and medical director of the Asian Medical Centre, which is affiliated with the University of Calgary Medical Clinic in Alberta, Canada. He graduated from the University of Hong Kong and completed an internship at Queen Mary Hospital, both in Hong Kong. He completed a residency in pediatrics at the University of Calgary.

HELEN CHO, M.D., is a family physician at the Asian Medical Centre in Calgary. Dr. Cho graduated from the University of Alberta in Edmonton, Alberta, and completed a residency in family medicine at the Royal Alexandra Hospital, also in Edmonton.

Address correspondence to Alexander K.C. Leung, M.B.B.S., Alberta Children's Hospital, 1820 Richmond Rd. S.W., Calgary, Alberta, Canada T2T 5C7. Reprints are not available from the authors.


(1.) Simon NP. Evaluation and management of stridor in the newborn. Clin Pediatr 1991;30:211-6.

(2.) Clough J. Managing stridor in children. Practitioner 1995;239(1557):724-8.

(3.) Gilbert EG, Russell KE, Deskin RW. Stridor in the infant and child. Assessment, treatment. AORN J 1993;58:23-37.

(4.) Skolnik N. Croup. J Fam Pract 1993;37(2):165-70.

(5.) Leung AK, Jadavji T. Polysaccharide vaccine for prevention of Haemophilus influenzae type b disease. J Roy Soc Health 1988;108:180-1.

(6.) Orenstein DM. Acute inflammatory upper airway obstruction. In: Nelson WE, Behrman RE, Kliegman RM, Arvin AM, eds. Nelson Textbook of pediatrics. Philadelphia: W.B. Saunders, 1996:1201-5.

(7.) Lesperance MM, Zalzal GH. Assessment and management of laryngotracheal stenosis. Pediatr Clin North Am 1996;43:1413-27.

(8.) Friedberg J. An approach to stridor in infants and children. J Otolaryngol 1987;16:203-6.

(9.) Sharief N, Matthew DJ, Dillon MJ. Hypocalcaemic stridor in children. How often is it missed? Clin Pediatr 1991;30:51-2.

(10.) LaRouere MJ, Koopmann CF Jr. Non-organic stridor in children. Int J Pediatr Otorhinolaryngol 1987;14: 73-7.

(11.) Cogbill TH, Moore FA, Accurso FJ, Lilly JR. Primary tracheomalacia. Ann Thorac Surg 1983;35:538-41.

(12.) Tunkel DE, Zalzal GH. Stridor in infants and children: ambulatory evaluation and operative diagnosis. Clin Pediatr 1992;31:48-55.

(13.) Handler SD. Stridor. In: Fleisher GR, Ludwig S, eds. Textbook of pediatric emergency medicine. Baltimore: Williams & Wilkins, 1993:474-8.

COPYRIGHT 1999 American Academy of Family Physicians
COPYRIGHT 2000 Gale Group

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